Examination Preparation
MCQs
Question 1:
Which of the following features best differentiates acute disseminated encephalomyelitis (ADEM) from multiple sclerosis (MS) at initial presentation?
Presence of oligoclonal bands in the CSF
Large, poorly demarcated bilateral white matter lesions on MRI
Optic neuritis as the sole presenting feature
Relapsing-remitting course with discrete attacks
Answer: (B) ADEM typically presents with large, bilateral, poorly demarcated bilateral white matter lesions on MRI
Question 2:
Which of the following findings is most characteristic of AIDP? dissociation in CSF
Rapidly ascending symmetric weakness with hyperreflexia
Progressive weakness with areflexia and albuminocytologic
Fluctuating weakness with preserved reflexes and fatigability
Sensory ataxia with preserved motor strength
Answer: (B) Progressive weakness with areflexia and albuminocytologic dissociation in CSF
Question 3:
Which of the following is most characteristic of Wernicke encephalopathy?
Peripheral neuropathy and optic neuritis
Ophthalmoplegia, ataxia, and confusion
Seizures and hemiparesis
Spastic paraparesis and cognitive decline
Answer: (B) The classic triad of ophthalmoplegia, ataxia, and confusion is seen in Wernicke’s Encephalopathy
Question 4:
Which of the following CSF findings is most characteristic of Alzheimer’s disease?
Increased A\(\beta\)42, decreased tau
Decreased A\(\beta\)42, increased phosphorylated tau
Increased A\(\beta\)42, normal tau
Normal A\(\beta\)42, increased tau
Answer: (B) Decreased A\(\beta\)42, increased phosphorylated tau
Question 5:
Which of the following imaging findings is most characteristic of cerebral amyloid angiopathy? susceptibility-weighted MRI
Deep basal ganglia hemorrhage with microbleeds in the thalamus
Lobar microbleeds and cortical superficial siderosis on
Subarachnoid hemorrhage with perimesencephalic distribution
Diffuse leukoencephalopathy without hemorrhagic lesions
Answer: (B) Lobar microbleeds and cortical superficial siderosis on susceptibility weighted imaging on MRI
Question 6:
Which of the following is a typical feature of amyloid neuropathy?
Rapid onset asymmetric neuropathy with preserved autonomic function
Length-dependent symmetric sensorimotor neuropathy with prominent autonomic involvement
Pure motor neuropathy with brisk reflexes
Demyelinating neuropathy with conduction block
Answer: (B) Length-dependent symmetric sensorimotor neuropathy with prominent autonomic involvement
Question 7:
Which of the following findings is most characteristic of ALS?
Sensory loss and absent reflexes
Ocular motility restriction and sphincter incontinence
Coexistence of upper and lower motor neuron signs in the same limb
Symmetric proximal weakness with myalgia
Answer: (C) Coexistence of upper and lower motor neuron signs in the same limb.
Question 8:
Which brain region is most susceptible to injury in anoxic brain injury?
Thalamus
Hippocampus
Pons
Occipital lobe
Answer: (B) Hippocampus.
Question 9:
Which of the following findings is most characteristic of anterior interosseous nerve syndrome?
Loss of thumb abduction
Sensory loss over the lateral three and a half fingers
Weakness of flexor pollicis longus and index finger flexion without
sensory loss
Loss of wrist extension
Answer: (C) Weakness of flexor pollicis longus and index finger flexion without sensory loss.
Question 10:
Which MRI finding is most characteristic of chronic arachnoiditis?
Diffuse spinal cord swelling
"Empty thecal sac" sign with nerve root clumping
Intramedullary ring-enhancing lesions
Disc herniation with foraminal narrowing
Answer: (B) "Empty thecal sac" sign with nerve root clumping.
Question 11:
Which of the following is the most characteristic clinical feature of Arnold–Chiari malformation type I?
Severe visual loss with optic neuritis
Headache exacerbated by coughing or Valsalva maneuvers
Rapidly progressive dementia
Peripheral neuropathy with glove-and-stocking distribution
Answer: (B) Headache exacerbated by coughing or Valsalva maneuvers.
Question 12:
Which of the following clinical features is most characteristic of chronic arsenic toxicity?
Proximal muscle weakness with preserved reflexes
Rapidly progressive optic neuritis
Painful, distal sensorimotor polyneuropathy with skin
hyperpigmentation
Acute cerebellar ataxia with nystagmus
Answer: (C) Painful, distal sensorimotor polyneuropathy with skin hyperpigmentation.
Question 13:
Which of the following findings is most characteristic of Autoimmune Autonomic Gangliopathy?
Symmetric sensorimotor polyneuropathy with distal weakness
Acute flaccid paralysis with preserved reflexes
Severe orthostatic hypotension with preserved motor and sensory function
Rapidly progressive cerebellar ataxia with ophthalmoplegia
Answer: (C) Severe orthostatic hypotension with preserved motor and sensory function.
Question 14:
Which of the following findings is most characteristic of anti-NMDA receptor encephalitis?
Rapidly progressive cerebellar ataxia with Purkinje cell loss
Subacute psychiatric symptoms followed by dyskinesias and autonomic instability
Acute ascending weakness with albuminocytologic dissociation
Sudden onset hemiparesis with restricted diffusion on MRI
Answer: (B) Subacute psychiatric symptoms followed by dyskinesias and autonomic instability are classic for anti-NMDA receptor encephalitis.
Question 15:
Which of the following findings is most characteristic of axillary nerve injury?
Weakness of elbow flexion and sensory loss over the lateral forearm
Weakness of shoulder abduction beyond 15\(^\circ\) and numbness over the lateral shoulder
Wasting of supraspinatus and infraspinatus with preserved deltoid strength
Loss of wrist extension with sensory loss over the dorsal hand
Answer: (B) Weakness of shoulder abduction beyond 15\(^\circ\) and numbness over the lateral shoulder.
Question 16:
Which of the following is the most strongly associated etiological factor in Bell’s palsy?
Epstein–Barr virus infection
Herpes simplex virus type 1 reactivation
Varicella-zoster virus reactivation
Autoimmune demyelination
Answer: (B) Herpes simplex virus type 1 reactivation
Question 17:
Which of the following is the most characteristic finding of posterior canal BPPV?
Persistent downbeat nystagmus without positional trigger
Vertigo lasting several hours with hearing loss
Vertigo lasting seconds with upbeat torsional nystagmus on
Dix-Hallpike maneuver
Horizontal nystagmus on caloric testing
Answer: (C) Vertigo lasting seconds with upbeat torsional nystagmus on Dix-Hallpike maneuver.
Question 18:
Which of the following findings best differentiates botulism from Guillain-Barré syndrome (AIDP)?
Presence of areflexia
Sensory loss
Cranial nerve involvement
Normal sensory examination with descending paralysis
Answer: (D) Normal sensory examination with descending paralysis
Question 19:
Which of the following findings most strongly suggests a preganglionic brachial plexus injury?
Absence of biceps reflex
Deltoid muscle wasting
Presence of Horner’s syndrome
Sensory loss over the thumb
Answer: (C) Presence of Horner’s syndrome – This finding indicates involvement proximal to the dorsal root ganglion, suggesting a preganglionic lesion.
Question 20:
Which of the following imaging findings is most characteristic of a brain abscess?
Homogeneous enhancement on contrast MRI
Ring-enhancing lesion with restricted diffusion on DWI
Calcified mass with surrounding gliosis
Hypodense lesion with no mass effect
Answer: (B) Ring-enhancing lesion with restricted diffusion on DWI is characteristic of a brain abscess and helps distinguish it from neoplastic lesions.
Question 21:
Which of the following findings most strongly supports a diagnosis of carpal tunnel syndrome?
Sensory loss in the little finger
Thenar muscle atrophy with preserved hypothenar strength
Proximal forearm pain radiating to the shoulder
Loss of the triceps reflex
Answer: (B) Thenar muscle atrophy with preserved hypothenar strength
Question 22:
Which of the following clinical findings is most specific for cauda equina syndrome?
Severe low back pain
Bilateral leg weakness
Saddle anesthesia
Urinary urgency
Answer: (C) Saddle anesthesia is the most specific sign of cauda equina syndrome and strongly indicates lumbosacral nerve root involvement.
Question 23:
Which cranial nerve is most commonly affected first in cavernous sinus thrombosis?
Oculomotor nerve (CN III)
Trochlear nerve (CN IV)
Trigeminal nerve (V1)
Abducens nerve (CN VI)
Answer: (D) Abducens nerve (CN VI) is often the first to be affected.
Question 24:
Which of the following findings is most characteristic of central retinal artery occlusion?
Flame-shaped hemorrhages and dilated veins
Cherry-red spot on the macula and pale retina
Optic disc swelling with peripapillary hemorrhages
Cotton wool spots and microaneurysms
Answer: (B) A cherry-red spot on the macula with a pale, edematous retina is the classic finding in central retinal artery occlusion.
Question 25:
Which of the following factors is most strongly associated with the formation of a cerebral (saccular) aneurysm?
Chronic hypertension
Cigarette smoking
Oral contraceptive use
Diabetes mellitus
Answer: (B) Cigarette smoking.
Question 26:
Which of the following findings is most characteristic of spastic diplegic cerebral palsy?
Flaccid paralysis of the lower limbs with absent reflexes
Progressive muscle weakness with fasciculations
Scissoring gait with increased tone and hyperreflexia in the legs
Rapidly progressive dystonia and cognitive decline
Answer: (C) Scissoring gait with increased tone and hyperreflexia in the legs
Question 27:
Which of the following statements regarding cerebral venous sinus thrombosis is TRUE?
Anticoagulation is contraindicated in the presence of intracerebral hemorrhage.
Headache is an uncommon presenting feature of CVST.
MR venography is the gold standard for diagnosis.
CVST most commonly affects elderly men with atherosclerosis.
Answer: (C) MR venography is the gold standard for diagnosis.
Question 28:
Which of the following is the most effective first-line treatment for cervical dystonia?
Oral baclofen
Botulinum toxin injection
Deep brain stimulation
Levodopa
Answer: (B) Botulinum toxin injection
Question 29:
Which of the following clinical findings most strongly suggests cervical myelopathy over peripheral neuropathy?
Distal sensory loss in a stocking-glove distribution
Hyporeflexia in the lower extremities
Positive Babinski sign
Reduced ankle jerk reflexes
Answer: (C) Positive Babinski sign
Question 30:
Which of the following findings is most characteristic of Charcot-Marie-Tooth disease?
Asymmetric proximal weakness with brisk reflexes
Symmetric distal weakness with pes cavus and reduced reflexes
Acute onset of ascending weakness and areflexia
Sensory neuronopathy with profound proprioceptive loss
Answer: (B) Symmetric distal weakness with pes cavus and reduced reflexes is the hallmark of Charcot-Marie-Tooth disease.
Question 31:
Which of the following findings is most characteristic of CIDP compared to AIDP (Guillain-Barré syndrome)?
Rapid progression of weakness over 7 days
Albuminocytologic dissociation in CSF
Relapsing course with symmetric sensorimotor involvement over 3 months
Predominant cranial nerve involvement
Answer: (C) CIDP is characterized by a chronic or relapsing course with progression beyond 8 weeks, distinguishing it from AIDP.
Question 32:
Which of the following MRI features is most characteristic of CLIPPERS?
Ring-enhancing lesions with central necrosis
Diffuse white matter hyperintensities sparing the brainstem
Punctate, pepper-like gadolinium-enhancing lesions in the pons
Cortical ribboning with restricted diffusion
Answer: (C) Punctate, pepper-like gadolinium-enhancing lesions in the pons.
Question 33:
Which of the following is considered first-line preventive therapy for cluster headache?
Topiramate
Propranolol
Verapamil
Indomethacin
Answer: (C) Verapamil is the first-line preventive agent for cluster headaches, requiring ECG monitoring during dose titration.
Question 34:
Which of the following best describes the pathophysiology of CRPS?
Primary demyelination of peripheral nerves
Autoimmune attack on synovial tissue
Aberrant neuroinflammatory and sympathetic response following tissue injury
Ischemic necrosis due to arterial occlusion
Answer: (C) Aberrant neuroinflammatory and sympathetic response following tissue injury
Question 35:
Which of the following clinical features most strongly suggests corticobasal syndrome?
Symmetric resting tremor responsive to levodopa
Alien limb phenomenon with cortical sensory loss
Vertical gaze palsy and early postural instability
Early memory loss with preserved motor function
Answer: (B) Alien limb phenomenon with cortical sensory loss
Question 36:
Which of the following findings is most characteristic of sporadic Creutzfeldt-Jakob disease?
MRI showing temporal lobe hyperintensity and CSF NMDA receptor antibodies
CSF positive for 14-3-3 protein and periodic sharp wave complexes on
EEG
Progressive memory decline with hippocampal atrophy on MRI over 5 years
Answer: (B) CSF positive for 14-3-3 protein and periodic sharp wave complexes on EEG
Question 37:
Which of the following findings is most characteristic of critical illness myopathy?
Asymmetric distal weakness with sensory loss
Normal muscle biopsy with demyelinating changes on nerve conduction
Symmetric proximal weakness with preserved sensation
Rapidly fluctuating ptosis and diplopia
Answer: (C) Symmetric proximal weakness with preserved sensation
Question 38:
Which of the following is the most characteristic feature of critical illness neuropathy?
Rapidly ascending paralysis with albuminocytologic dissociation
Symmetric distal weakness with reduced CMAPs and preserved sensory potentials
Predominant bulbar involvement with ophthalmoplegia
Sensory ataxia with areflexia and severe proprioceptive loss
Answer: (B) Symmetric distal weakness with reduced CMAPs and preserved sensory potentials
Question 39:
Which clinical feature most strongly suggests advanced cubital tunnel syndrome?
Positive Phalen’s sign
Atrophy of hypothenar muscles with clawing of the fourth and fifth
digits
Loss of sensation in the radial three and a half digits
Wrist drop with inability to extend fingers
Answer: (B) Atrophy of hypothenar muscles with clawing of the fourth and fifth digits
Question 40:
Which histopathological feature is most characteristic of dermatomyositis?
Endomysial inflammation with CD8+ T cells
Rimmed vacuoles and inclusion bodies
Perifascicular atrophy with perivascular inflammation
Necrotizing vasculitis with fibrinoid necrosis
Answer: (C) Perifascicular atrophy with perivascular inflammation
Question 41:
Which of the following findings is most characteristic of diabetic amyotrophy?
Symmetric distal sensory loss with preserved strength
Proximal thigh pain followed by asymmetric weakness and muscle
wasting
Rapidly progressive bulbar weakness and fasciculations
Severe orthostatic hypotension with absent sweat response
Answer: (B) Proximal thigh pain followed by asymmetric weakness and
Question 42:
Which of the following is the most common clinical presentation of diabetic neuropathy?
Acute mononeuropathy
Proximal motor neuropathy
Symmetric distal sensorimotor polyneuropathy
Cranial nerve palsy
Answer: (C) Symmetric distal sensorimotor polyneuropathy
Question 43:
Which of the following features is most characteristic of DADS
associated with IgM monoclonal gammopathy?
Rapid progression with proximal weakness
Severe autonomic dysfunction
Predominant distal sensory involvement with anti-MAG antibodies
Frequent cranial nerve palsies
Answer: (D) Predominant distal sensory involvement with anti-MAG antibodies
Question 44:
Which of the following MRI findings is most characteristic of herpes simplex encephalitis?
Bilateral occipital lobe hyperintensity
Unilateral temporal lobe FLAIR hyperintensity with hemorrhagic features
Symmetric thalamic involvement
Diffuse cortical demyelination
Answer: (B) Unilateral temporal lobe FLAIR hyperintensity with hemorrhagic features
Question 45:
Which of the following is considered a first-line treatment for essential tremor?
Levodopa
Propranolol
Amantadine
Ropinirole
Answer: (B) Propranolol
Question 46:
Which of the following EEG findings is most characteristic of primary generalized epilepsy?
Focal sharp waves over the temporal lobe
Periodic lateralized epileptiform discharges (PLEDs)
Triphasic waves
Generalized spike-and-wave discharges
Answer: (D) Generalized spike-and-wave discharges
Question 47:
Which of the following is a characteristic clinical feature of Fabry’s disease?
Early-onset proximal muscle weakness
Angiokeratomas in the lower trunk and genital region
Cerebellar ataxia with demyelinating neuropathy
Bilateral optic neuritis
Answer: (B) Angiokeratomas in the lower trunk and genital region
Question 48:
Which of the following is a characteristic clinical feature of facioscapulohumeral muscular dystrophy (FSHD)?
Early involvement of distal lower limb muscles
Symmetric limb weakness with early respiratory failure
Asymmetric weakness involving facial and shoulder muscles
Severe cardiac involvement in early stages
Answer: (C) Asymmetric weakness involving facial and shoulder muscles
Question 49:
Which of the following clinical findings is most characteristic of femoral neuropathy?
Foot drop with sensory loss over the dorsum of the foot
Weakness of knee extension with absent patellar reflex
Loss of ankle jerk with calf atrophy
Sensory loss in the perineal region with urinary incontinence
Answer: (B) Weakness of knee extension with absent patellar reflex
Question 50:
Which of the following best explains the underlying mechanism of fibromyalgia?
Autoimmune-mediated inflammation of muscle tissue
Central nervous system amplification of pain signaling
Demyelination of peripheral nerves
Synovial inflammation of large joints
Answer: (B) Central nervous system amplification of pain signaling
Question 51:
Which of the following genetic findings is diagnostic of Fragile X syndrome?
CGG repeat expansion >200 in the FMR1 gene with promoter
methylation
GAA repeat expansion in the FXN gene
CAG repeat expansion in the HTT gene
Deletion of 15q11-q13 region
Answer: (A) CGG repeat expansion >200 in the FMR1 gene with promoter
Question 52:
What is the genetic defect responsible for Friedreich’s ataxia?
CGG repeat expansion in the FMR1 gene
GAA repeat expansion in the FXN gene
CAG repeat expansion in the ATXN3 gene
CTG repeat expansion in the DMPK gene
Answer: (B) GAA repeat expansion in the FXN gene
Question 53:
Which of the following features most strongly suggests frontotemporal dementia over Alzheimer’s disease?
Early prominent memory impairment
Visual hallucinations
Social disinhibition and loss of empathy
Fluctuating cognition
Answer: (C) Social disinhibition and loss of empathy
Question 54:
Which of the following findings is most characteristic of genitofemoral neuralgia?
Motor weakness in the quadriceps muscle
Burning pain radiating to the medial calf
Sharp inguinal and genital pain worsened by hip extension
Sensory loss in the perianal region
Answer: (C) Sharp inguinal and genital pain worsened by hip extension.
Question 55:
Which of the following features is most characteristic of glossopharyngeal neuralgia?
Continuous dull pain in the maxillary region
Stabbing pain triggered by swallowing and radiating to the ear
Numbness of the anterior two-thirds of the tongue
Bilateral constant burning pain in the mandible
Answer: (B) Stabbing pain triggered by swallowing and radiating to the ear.
Question 56:
Which of the following is the most characteristic feature of HaNDL syndrome?
Chronic, progressive headaches with papilledema
Recurrent headaches with transient focal neurological deficits and CSF lymphocytosis
Visual hallucinations and cognitive decline with abnormal MRI
Persistent hemiparesis and elevated protein without pleocytosis
Answer: (B) Recurrent headaches with transient focal neurological deficits and CSF lymphocytosis
Question 57:
Which of the following findings most reliably distinguishes hemifacial spasm from tics?
Presence of pain during spasms
Occurrence during sleep
Bilateral facial involvement
Association with sensory deficits
Answer: (B) Occurrence during sleep
Question 58:
Which of the following findings most reliably distinguishes pure hereditary spastic paraplegia from complex forms?
Presence of optic atrophy
Absence of sensory loss and cerebellar signs
Early onset before age 10
Rapid progression with upper limb involvement
Answer: (B) Absence of sensory loss and cerebellar signs
Question 59:
Which of the following findings is most characteristic of Holmes-Adie Syndrome?
Bilateral pinpoint pupils with intact light response
Dilated pupil with slow constriction to near effort and absent Achilles reflexes
Rapidly reactive pupils with preserved deep tendon reflexes
Fixed mid-position pupils unresponsive to light or near effort
Answer: (B) Dilated pupil with slow constriction to near effort and absent Achilles reflexes
Question 60:
Which of the following features is most characteristic of hyperkalemic periodic paralysis?
Prolonged episodes of paralysis triggered by carbohydrate-rich meals
Short episodes of weakness associated with elevated serum potassium
Symmetric paralysis lasting several days with hypokalemia
Frequent respiratory involvement during attacks
Answer: (B) Short episodes of weakness associated with elevated serum potassium
Question 61:
Which of the following is the most common precipitating factor for attacks of hypokalemic periodic paralysis?
Fasting
Heavy carbohydrate meal followed by rest
Prolonged exercise without rest
Infection
Answer: (B) Heavy carbohydrate meal followed by rest
Question 62:
Which of the following is a hallmark histopathologic feature of IgG4-related disease?
Caseating granulomas
Perivascular demyelination
Storiform fibrosis with IgG4-positive plasma cells
Amyloid deposition
Answer: (C). Storiform fibrosis with IgG4-positive plasma cells
Question 63:
Which of the following features is most characteristic of immune checkpoint inhibitor-associated myasthenia gravis compared to idiopathic myasthenia gravis?
Presence of thymoma
Gradual onset over several years
Frequent association with myositis or myocarditis
Predominantly sensory neuropathy
Answer: (C) Frequent association with myositis or myocarditis
Question 64:
Which of the following is most characteristic of inclusion body myositis?
Rapidly progressive symmetric proximal muscle weakness
Presence of anti-Mi-2 antibodies
Asymmetric involvement of quadriceps and finger flexors with rimmed vacuoles on biopsy
Dramatic improvement with corticosteroid therapy
Answer: (C) Asymmetric involvement of quadriceps and finger flexors with rimmed vacuoles on biopsy is the hallmark of IBM. Unlike other inflammatory myopathies, IBM presents with asymmetric distal and proximal weakness, is refractory to immunosuppression, and requires all three pathological features (inflammation, rimmed vacuoles, protein inclusions) for definite diagnosis.
Question 65:
Which of the following findings is most characteristic of Jugular Foramen Syndrome?
Bilateral ophthalmoplegia with ptosis
Dysphagia, hoarseness, and shoulder weakness
Trigeminal neuralgia with facial numbness
Facial paralysis with hearing loss
Answer: (B) Dysphagia, hoarseness, and shoulder weakness due to IX, X, XI involvement
Question 66:
Which of the following neuropathological features is characteristic of kuru?
Demyelination with macrophage infiltration
Spongiform degeneration with PrP deposition
Neuronal necrosis with neutrophilic inflammation
Lymphocytic perivascular cuffing
Answer: (B) Spongiform degeneration with PrP deposition.Kuru is a prion disease characterized by spongiform changes, neuronal loss, and accumulation of abnormal prion protein in the cerebellum and brainstem without inflammatory response.
Question 67:
Which of the following findings best differentiates Lambert–Eaton myasthenic syndrome (LEMS) from myasthenia gravis?
Presence of ptosis and diplopia early in disease
Incremental increase in CMAP amplitude after high-frequency stimulation
Decremental response to low-frequency repetitive nerve stimulation
Positive acetylcholine receptor antibodies
Answer: (B) Incremental increase in CMAP amplitude after high-frequency stimulation is characteristic of LEMS and helps differentiate it from myasthenia gravis.
Question 68:
Which of the following features most strongly supports a diagnosis of Lewy body dementia over Alzheimer’s disease?
Early memory loss with hippocampal atrophy on MRI
Fluctuating cognition, recurrent visual hallucinations, and
parkinsonism occurring within one year of each other
Gradual visuospatial decline without hallucinations
Stepwise progression of cognitive deficits
Answer: (B) Fluctuating cognition, recurrent visual hallucinations, and arkinsonism occurring within one year of each other are classic features of Lewy body dementia.
Question 69:
Which of the following features most strongly suggests a diagnosis of limb-girdle muscular dystrophy (LGMD)?
Sensory loss with distal muscle weakness
Fluctuating weakness with fatigability
Symmetrical proximal muscle weakness with elevated CK
Rapid progression with ocular involvement
Answer: (C) Symmetrical proximal muscle weakness with elevated CK is characteristic of LGM
Question 70:
Which of the following findings is most characteristic of spontaneous intracranial hypotension?
Headache that worsens with lying down and improves when upright
Diffuse pachymeningeal enhancement with orthostatic headache
Sudden thunderclap headache with normal MRI findings
Headache associated with papilledema and elevated CSF pressure
Answer: (B) Diffuse pachymeningeal enhancement with orthostatic headache.
Question 71:
Which of the following clinical findings most strongly suggests lumbosacral plexopathy rather than lumbar radiculopathy?
Pain radiating down the posterior leg in an S1 distribution
Weakness confined to hip flexors with dermatomal sensory loss
Patchy sensory deficits involving multiple non-dermatomal regions
Isolated absent ankle reflex with plantar flexion weakness
Answer: (C) Patchy sensory deficits involving multiple non-dermatomal regions.
Question 72:
Which of the following autoantibodies is most strongly associated with neuropsychiatric lupus?
Anti-centromere antibody
Anti-ribosomal P antibody
Anti-mitochondrial antibody
Anti-Jo-1 antibody
Answer: (B) Anti-ribosomal P antibody.
Question 73:
Which of the following clinical findings is most characteristic of Lyme neuroborreliosis?
Rapidly progressive dementia with spastic paraparesis
Painful radiculopathy with lymphocytic meningitis weeks after a tick bite
Flaccid paralysis with albuminocytologic dissociation
Sudden-onset hemiparesis and aphasia due to large-vessel occlusion
Answer: (B) Painful radiculopathy with lymphocytic meningitis weeks after a tick bite.
Question 74:
Which of the following features is most characteristic of primary CNS ymphoma on MRI?
Heterogeneous ring enhancement with central necrosis
Homogeneous enhancement with periventricular localization and restricted diffusion
Non-enhancing lesion with diffuse white matter involvement
Peripheral cortical lesion with blooming on susceptibility imaging
Answer: (B) Homogeneous enhancement with periventricular localization and restricted diffusion.
Question 75:
A 57-year-old man presents with nausea, vomiting, hiccups, left-sided weakness, and tongue deviation to the right. MRI shows a right medial medullary infarct. Which artery is most likely occluded?
Posterior inferior cerebellar artery
Anterior spinal artery
Basilar artery
Superior cerebellar artery
Answer: (B) Anterior spinal artery
Question 76:
Which of the following features best distinguishes stroke-like episodes in MELAS from typical ischemic strokes?
Onset before age 40 with sudden focal neurological deficits
Elevated serum lactate during acute episodes
Cortical involvement with hemiparesis and aphasia
MRI lesions confined to the territory of the middle cerebral artery
Answer: (B) Elevated serum lactate during acute episodes Stroke-like episodes in MELAS are metabolic in origin, associated with lactic acidosis, and the lesions typically do not conform to vascular territories.
Question 77:
Which of the following MRI features is most characteristic of a meningioma?
Ring-enhancing lesion with central necrosis
Extra-axial mass with dural tail and homogeneous enhancement
Butterfly-shaped lesion crossing the corpus callosum
Irregular intra-axial lesion with poor enhancement
Answer: (B) Extra-axial mass with dural tail and homogeneous enhancement.This imaging pattern strongly suggests a meningioma due to its duralattachment and vascularity.
Question 78:
Which of the following cerebrospinal fluid (CSF) findings is most characteristic of bacterial meningitis?
Lymphocytic pleocytosis, normal glucose, mildly elevated protein
Neutrophilic pleocytosis, low glucose, elevated protein
Lymphocytic pleocytosis, low glucose, elevated protein
Eosinophilic pleocytosis, normal glucose, elevated protein
Answer: (B) Neutrophilic pleocytosis, low glucose, elevated protein This CSF profile is classic for bacterial meningitis due to the intense neutrophilic inflammatory response and increased metabolic consumption of glucose.
Question 79:
Which of the following clinical features most strongly suggests meralgia paresthetica rather than lumbar radiculopathy?
Pain radiating from the back into the thigh with associated knee extension weakness
Burning and tingling localized to the anterolateral thigh without motor weakness
Sensory loss in the medial thigh accompanied by hip flexor weakness
Absent patellar reflex and sensory loss over the anterior knee
Answer: (B) Burning and tingling localized to the anterolateral thigh without motor weakness Meralgia paresthetica is characterized by a purely sensory disturbance in the distribution of the lateral femoral cutaneous nerve.
Question 80:
Which of the following is most characteristic of MGUS-associated neuropathy?
Rapidly progressive asymmetric weakness with cranial nerve involvement
Distal symmetric demyelinating neuropathy associated with IgM paraprotein
Acute flaccid paralysis following infection
Sensory neuropathy with severe autonomic dysfunction
Answer: (B) Distal symmetric demyelinating neuropathy associated with IgM paraprotein
Question 81:
Which of the following features most strongly supports a diagnosis of migraine with aura rather than transient ischemic attack (TIA)?
Sudden onset of visual field loss without positive phenomena
Gradual progression of visual scintillations followed by headache
Unilateral headache lasting less than 30 minutes
Complete resolution of symptoms within 5 minutes
Answer: (B) Gradual progression of visual scintillations followed by headache Migraine aura typically develops gradually over 5–20 minutes,is often positive (e.g., visual scintillations), and is followed by a headache, whereas TIA is abrupt, negative, and often not followed by headache.
Question 82:
Which of the following features is most characteristic of Miller Fisher Syndrome?
Progressive ascending limb weakness with early respiratory
involvement
Bilateral ophthalmoplegia, ataxia, and areflexia with positive
anti-GQ1b antibodies
Sudden onset vertical gaze palsy with altered consciousness
Ptosis and fatigable weakness that improves with rest
Answer: (B) Bilateral ophthalmoplegia, ataxia, and areflexia with positive anti-GQ1b antibodies This triad, along with anti-GQ1b positivity, is highly characteristic of Miller Fisher Syndrome and helps distinguish it from other neuromuscular disorders such as classic GBS.
Question 83:
Which of the following features most strongly suggests mononeuritis multiplex?
Symmetric distal sensory neuropathy progressing slowly over years
Acute, asymmetric, multifocal involvement of non-contiguous nerves
Predominant demyelination with conduction block in multiple nerves
Pure motor neuropathy without sensory involvement
Answer: (B) Acute, asymmetric, multifocal involvement of non-contiguous nerves Mononeuritis multiplex classically presents with abrupt,asymmetric deficits involving multiple non-contiguous nerves due to ischemic infarction from vasculitic inflammation.
Question 84:
oindent Which of the following is most characteristic of Morvan disease?
Acute ascending paralysis with albuminocytologic dissociation
Neuromyotonia with severe insomnia, dysautonomia, and anti-CASPR2 antibodies
Flaccid paralysis after exposure to botulinum toxin
Visual hallucinations and parkinsonism due to basal ganglia lesions
Answer: (B) Neuromyotonia with severe insomnia, dysautonomia, and anti-CASPR2 antibodies This constellation of features, especially with VGKC-complex antibodies, is highly specific for Morvan disease.
Question 85:
oindent Which of the following angiographic findings is most characteristic of Moyamoya disease?
Segmental beading of medium-sized arteries
“Puff of smoke” appearance from basal collateral networks
Fusiform aneurysm of the posterior circulation
String-of-pearls appearance in the extracranial carotid artery
Answer: (B) “Puff of smoke” appearance from basal collateral networks,This appearance on angiography is the hallmark of Moyamoya disease,representing proliferative collateral vessels in response to progressive intracranial arterial stenosis.
Question 86:
Which of the following features most strongly distinguishes MADSAM from ultifocal motor neuropathy (MMN)?
Presence of conduction block on nerve conduction studies
Asymmetric, multifocal involvement of peripheral nerves
Prominent sensory symptoms and deficits
Response to intravenous immunoglobulin (IVIg)
Answer: (C) Prominent sensory symptoms and deficits MADSAM typically affects both motor and sensory fibers, whereas MMN is characterized by purely motor involvement.
Question 87:
Which of the following features most strongly supports a diagnosis of multifocal motor neuropathy rather than amyotrophic lateral sclerosis (ALS)?
Presence of upper motor neuron signs
Symmetric proximal weakness
Conduction block on motor nerve conduction studies without sensory involvement
Rapid progression with bulbar involvement
Answer: (C) Conduction block on motor nerve conduction studies without sensory involvement. This electrophysiologic finding is characteristic of MMN and differentiates it from ALS, which shows diffuse lower and upper motor neuron involvement without conduction block.
Question 88:
Which of the following MRI findings is most characteristic of multiple Sclerosis?
Symmetrical basal ganglia calcifications
Ovoid periventricular lesions oriented perpendicular to the ventricles (Dawson’s fingers)
Cortical ribbon hyperintensity on T1-weighted imaging
Ring-enhancing lesions with central necrosis
Answer: (B) Ovoid periventricular lesions oriented perpendicular to the ventricles (Dawson’s fingers) These lesions reflect demyelinating plaques along medullary veins and are a hallmark imaging feature of MS.
Question 89:
Which of the following best describes the primary pathophysiological defect in Duchenne muscular dystrophy?
Loss of acetylcholine receptors at the neuromuscular junction
Absence of dystrophin leading to sarcolemmal instability
Autoimmune-mediated inflammation of muscle fibers
Defective mitochondrial oxidative phosphorylation
Answer: (B) Absence of dystrophin leading to sarcolemmal instability
Question 90:
Which of the following best distinguishes myasthenia gravis from Lambert-Eaton myasthenic syndrome (LEMS)?
Presence of proximal muscle weakness
Presence of ocular symptoms such as ptosis and diplopia
Improvement of strength with repeated stimulation
Association with malignancy
Answer: (B) Presence of ocular symptoms such as ptosis and diplopia Ocular involvement is characteristic of MG and rare in LEMS, which typically improves with repeated activity due to presynaptic facilitation.
Question 91:
Which of the following features most reliably distinguishes MOGAD from AQP4-positive NMOSD?
Presence of longitudinally extensive transverse myelitis
Severe optic neuritis
Good visual recovery and steroid responsiveness
Female predominance
Answer: (C) Good visual recovery and steroid responsiveness While both diseases can cause optic neuritis and extensive myelitis, MOGAD is characterized by better recovery and higher responsiveness to corticosteroids compared to AQP4-positive NMOS
Question 92:
Which of the following findings best distinguishes myopathy from neuropathy?
Proximal muscle weakness with preserved reflexes
Muscle atrophy and fasciculations
Loss of vibration and proprioception
Distal muscle weakness and sensory loss
Answer: (A) Proximal muscle weakness with preserved reflexes Myopathies characteristically present with proximal weakness and preserved reflexes and sensation, whereas neuropathies typically cause distal weakness, sensory deficits, and reduced reflexes.
Question 93:
Which of the following findings is most characteristic of dermatomyositis compared to polymyositis?
Endomysial CD8\(^{+}\) T-cell infiltration
Perivascular inflammation with complement deposition
Rimmed vacuoles with protein inclusions
Distal asymmetric muscle weakness
Answer: (B) Perivascular inflammation with complement deposition. Dermatomyositis is distinguished by perivascular and perifascicular inflammation, complement activation, and characteristic cutaneous manifestations, whereas polymyositis shows endomysial CD8\(^{+}\) T-cell infiltration.
Question 94:
Which of the following clinical features best distinguishes myotonia congenita from paramyotonia congenita?
Muscle hypertrophy
Worsening of stiffness with repeated muscle activity
Association with CLCN1 gene mutation
Autosomal recessive inheritance pattern
Answer: (B) Worsening of stiffness with repeated muscle activity Myotonia congenita is characterized by the warm-up phenomenon, where stiffness improves with repeated activity, whereas paramyotonia congenita typically worsens with activity and cold exposure.
Question 95:
Which of the following findings is most characteristic of myotonic dystrophy?
Proximal muscle weakness with early contractures
Fluctuating muscle weakness worsened by activity
Difficulty releasing grip after handshakes and early cataracts
Rapidly progressive symmetric proximal weakness in childhood
Answer: (C) Difficulty releasing grip after handshakes and early cataracts — these are classic manifestations of myotonic dystrophy,reflecting myotonia and multisystem involvement.
Question 96:
Which of the following genetic mutations is most commonly associated with NARP syndrome?
POLG gene mutation
MT-ATP6 gene mutation
FXN gene mutation
OPA1 gene mutation
Answer: (B) MT-ATP6 gene mutation NARP syndrome is most often caused by a point mutation in the MT-ATP6 gene encoding a subunit of mitochondrial ATP synthase, leading to impaired oxidative phosphorylation.
Question 97:
Which of the following features most strongly suggests neuralgic amyotrophy rather than cervical radiculopathy?
Pain radiating from the neck to the arm with dermatomal sensory loss
Acute onset of severe shoulder pain followed days later by patcy muscle weakness
Muscle weakness accompanied by brisk reflexes and spasticity
Symmetric distal weakness and sensory loss in a stocking-glove distribution
Answer: (B) Acute onset of severe shoulder pain followed days later by patchy muscle weakness This temporal pattern is highly characteristic of neuralgic amyotrophy and differentiates it from cervical radiculopathy,
Question 98:
oindent Which of the following findings is most characteristic of Neurofibromatosis type 1?
Bilateral vestibular schwannomas
Multiple café-au-lait macules and axillary freckling
Ependymomas of the spinal cord
Multiple meningiomas without cutaneous involvement
Answer: (B) Multiple café-au-lait macules and axillary freckling
Question 99:
oindent Which of the following features most reliably distinguishes NMOSD from multiple sclerosis?
Presence of periventricular brain lesions
Oligoclonal bands in the cerebrospinal fluid
Longitudinally extensive spinal cord lesions involving three or more vertebral segments
Subcortical U-fiber lesions on brain MRI
Answer: (C) Longitudinally extensive spinal cord lesions involving three or more vertebral segments LETM is a hallmark of NMOSD and contrasts with the typically short-segment lesions seen in MS.
Question 100:
Which of the following clinical findings is most characteristic of tabes dorsalis in neurosyphilis?
Hyperreflexia and spastic paraparesis
Sensory ataxia with lightning pains
Fluctuating muscle weakness with fatigability
Bilateral internuclear ophthalmoplegia
Answer: (B) Sensory ataxia with lightning pains
Question 101:
Which of the following findings is most characteristic of non-arteritic anterior ischemic optic neuropathy (NAION)?
Painful vision loss with demyelinating lesions on MRI
Optic disc edema with peripapillary hemorrhages and altitudinal field defect
Bilateral simultaneous optic disc pallor and severe headache
Progressive, painless central vision loss over months
Answer: (B) Optic disc edema with peripapillary hemorrhages and altitudinal field defect.
Question 102:
Which of the following is a distinguishing clinical feature of occipital neuralgia?
Continuous dull bilateral headache associated with photophobia and nausea
Sudden, stabbing paroxysms of pain radiating from the occipital region towards the vertex
Pain predominantly located in the periorbital region with tearing and nasal congestion
Tension type headaches across the front of head.
Answer: (B) Sudden, stabbing paroxysms of pain radiating from the occipital region towards vertex
Question 103:
Which of the following findings best distinguishes ocular myasthenia gravis from a third nerve palsy?
Ptosis with pupillary involvement
Ophthalmoplegia with pain
Fluctuating ptosis and diplopia with normal pupils
Fixed, dilated pupil with impaired accommodation
Answer: (C) Fluctuating ptosis and diplopia with normal pupils
Question 104:
Which of the following best distinguishes oculopharyngeal muscular dystrophy (OPMD) from myasthenia gravis?
Presence of bilateral ptosis
Dysphagia affecting both solids and liquids
Slow, non-fluctuating progression of symptoms
Involvement of proximal limb muscles
Answer: (C) Slow, non-fluctuating progression of symptoms
Question 105:
Which of the following genetic alterations is characteristic of oligodendroglioma and has significant diagnostic and prognostic implications?
TP53 mutation
BRAF V600E mutation
1p/19q co-deletion
NF1 deletion
Answer: (C) 1p/19q co-deletion
Question 106:
Which bedside finding most supports neurogenic orthostatic hypotension?
SBP drop 22 mmHg and HR rise 30 bpm on standing
SBP drop 25 mmHg with HR rise only 4 bpm on standing
SBP drop 10 mmHg with HR rise 25 bpm on standing
SBP stable with HR rise 35 bpm on standing
Answer: (B) SBP drop 25 mmHg with minimal HR increase suggests impaired autonomic compensation (neurogenic).
Question 107:
Which of the following best characterizes orthostatic tremor?
A 4–6 Hz resting tremor affecting distal limbs, improving with movement
A high-frequency (13–18 Hz) synchronous tremor occurring exclusively while standing
A variable-frequency tremor suppressed by distraction and associated
with psychiatric illness
Answer: (B) A high-frequency (13–18 Hz) synchronous tremor occurring while standing
Question 108:
oindent Which of the following antibodies is most commonly associated with paraneoplastic cerebellar degeneration in a patient with breast cancer?
Anti-Hu (ANNA-1)
Anti-Yo (PCA-1)
Anti-Ri (ANNA-2)
Anti-Ma2
Answer: (B) Anti-Yo (PCA-1)
Question 109:
Which of the following features most strongly supports a diagnosis of idiopathic Parkinson’s disease?
Early postural instability within 6 months of onset
Rapid progression with poor response to levodopa
Symmetric onset of rigidity and tremor
Asymmetric onset with clear levodopa responsiveness
Answer: (D) Asymmetric onset with clear levodopa responsiveness
Question 110:
Which of the following features most strongly suggests a demyelinating rather than axonal peripheral neuropathy?
Length-dependent distal sensory loss
Significantly slowed nerve conduction velocity
Muscle wasting and fasciculations
Reduced compound motor action potential amplitude
Answer: (B) Significantly slowed nerve conduction velocity
Question 111:
Which of the following features most reliably distinguishes peroneal neuropathy at the fibular neck from L5 radiculopathy?
Foot drop
Sensory loss over the dorsum of the foot
Weakness of ankle dorsiflexion
Preservation of ankle inversion strength
Answer: (D) Preservation of ankle inversion strength
Question 112:
Which of the following clinical findings most strongly supports a diagnosis of piriformis syndrome rather than lumbar radiculopathy?
Weakness of ankle dorsiflexion
Positive straight leg raise test
Tenderness over the sciatic notch with pain on hip internal rotation
Dermatomal sensory loss in the L5 distribution
Answer: (C) Tenderness over the sciatic notch with pain on hip internal rotation.
Question 113:
oindent Which of the following is the first-line treatment for a macroprolactinoma?
Transsphenoidal surgical resection
Dopamine agonist therapy
External beam radiotherapy
Observation with periodic imaging
Answer: (B) Dopamine agonist therapy
Question 114:
Which of the following is the most immediate life-saving intervention in a patient presenting with pituitary apoplexy and hypotension?
Intravenous mannitol
Emergency transsphenoidal surgery
Intravenous corticosteroid therapy
Broad-spectrum antibiotics
Observation with serial imaging
Answer: (C) Intravenous corticosteroid therapy
Question 115:
Which of the following findings most strongly supports a diagnosis of POEMS syndrome over CIDP?
Symmetric sensorimotor polyneuropathy
Elevated VEGF levels and sclerotic bone lesions
Presence of anti-ganglioside antibodies
Rapid onset of weakness with cranial nerve involvement
Answer: (B) Elevated VEGF levels and sclerotic bone lesions
Question 116:
Which of the following features best distinguishes polymyalgia rheumatica from polymyositis?
Bilateral proximal muscle weakness
Elevated creatine kinase levels
Elevated ESR and CRP
Rapid response to low-dose corticosteroids
Answer: (D) Rapid response to low-dose corticosteroids
Question 117:
oindent Which of the following histopathological features is most characteristic of polymyositis?
Perifascicular atrophy with complement-mediated vascular damage
Endomysial infiltration by CD8T cells invading non-necrotic fibers
Rimmed vacuoles with protein inclusions
Granulomatous inflammation with multinucleated giant cells
Answer: (B) Endomysial infiltration by CD8 T cells invading non-necrotic fibers
Question 118:
Which of the following features best differentiates porphyria neuropathy from Guillain-Barré syndrome?
Presence of severe sensory loss and albuminocytologic dissociation
Predominantly motor axonal neuropathy with preserved sensation
Rapid onset following a viral illness
High cerebrospinal fluid protein with normal cell count
Answer: (B) Predominantly motor axonal neuropathy with preserved sensation
Question 119:
Which of the following best describes post-concussion syndrome (PCS)?
Structural brain injury with progressive neurological deterioration following traumatic brain injury
A chronic neurodegenerative condition characterized by abnormal protein aggregation
A constellation of cognitive, emotional, and somatic symptoms
persisting beyond the typical recovery period after a mild traumatic
Answer: (C) A constellation of cognitive, emotional, and somatic symptoms
Question 120:
Which of the following features most strongly supports a diagnosis of posterior cortical atrophy over typical Alzheimer’s disease?
Early impairment of episodic memory
Prominent visuospatial dysfunction with preserved visual acuity
Early aphasia and apraxia of speech
Parkinsonism and visual hallucinations
Answer: (B) Prominent visuospatial dysfunction with preserved visual acuity
Question 121:
Which of the following clinical findings best distinguishes posterior interosseous nerve syndrome from radial tunnel syndrome?
Pain in the lateral forearm during pronation
Paresthesia over the dorsum of the hand
Motor weakness of finger extension without sensory deficit
Tenderness over the lateral epicondyle
Answer: (C) Motor weakness of finger extension without sensory deficit
Question 122:
Which of the following MRI findings is most characteristic of PRES?
Restricted diffusion in the basal ganglia with hemorrhage
Bilateral parieto-occipital vasogenic edema on T2/FLAIR
Diffuse leptomeningeal enhancement with mass effect
Unilateral cortical infarction in the MCA territory
Answer: (B) Bilateral parieto-occipital vasogenic edema on T2/FLAIR PRES
Question 123:
Which of the following findings is most characteristic of POTS?
A sustained drop in systolic blood pressure of >20 mmHg within 3 minutes of standing
A sustained heart rate increase of >30 bpm within 10 minutes of standing without orthostatic hypotension
Sinus bradycardia during tilt-table testing
Absence of sympathetic activation upon standing
Answer: (B) A sustained heart rate increase of more than 30 bpm within 10 minutes of standing without orthostatic hypotension.
Question 124:
Which of the following findings is most suggestive of primary lateral sclerosis rather than amyotrophic lateral sclerosis?
Rapid progression to respiratory failure within 2 years
Presence of fasciculations on EMG
Slowly progressive spastic paraparesis without muscle atrophy
Mixed upper and lower motor neuron signs at onset
Answer: (C) Slowly progressive spastic paraparesis without muscle atrophy
Question 125:
Which of the following clinical features is most characteristic of the semantic variant of primary progressive aphasia?
Effortful, agrammatic speech with apraxia of speech
Word-finding pauses with impaired repetition
Fluent but empty speech with loss of word meaning
Early impairment of episodic memory
Answer: (C) Fluent but empty speech with loss of word meaning Semantic
Question 126:
Which of the following findings is most characteristic of sporadic Creutzfeldt-Jakob disease (sCJD)?
Rapidly progressive dementia over several years
Presence of oligoclonal bands in the CSF
Periodic sharp-wave complexes on EEG
Enhancement of basal ganglia on gadolinium MRI
Answer: (C) Periodic sharp-wave complexes on EEG
Question 127:
Which of the following MRI findings is most characteristic of PML?
Ring-enhancing lesions with mass effect
Multifocal white matter lesions without enhancement or mass effect
Basal ganglia involvement with hemorrhage
Periventricular lesions with gadolinium enhancement
Answer: (B) Multifocal white matter lesions without enhancement or mass effect.
Question 128:
Which of the following features most reliably distinguishes Progressive Muscular Atrophy from Amyotrophic Lateral Sclerosis at initial presentation?
Fasciculations
Hyperreflexia
Absence of upper motor neuron signs
Bulbar involvement
Answer: (C) Absence of upper motor neuron signs
Question 129:
Which of the following features most reliably distinguishes progressive supranuclear palsy from Parkinson’s disease?
Rest tremor
Early vertical gaze palsy
Bradykinesia
Levodopa responsiveness
Answer: (B) Early vertical gaze palsy Vertical supranuclear gaze palsy,
Question 130:
Which of the following findings is most characteristic of idiopathic intracranial hypertension (pseudotumor cerebri)?
Asymmetric limb weakness
Bilateral papilledema with normal CSF composition
Low CSF opening pressure on lumbar puncture
Ring-enhancing lesions on MRI
Answer: (B) Bilateral papilledema with normal CSF composition
Question 131:
Which of the following clinical features is most characteristic of pudendal neuralgia?
Perineal pain worsened by standing
Perineal pain that wakes the patient from sleep
Perineal pain relieved by sitting on a toilet seat
Presence of significant motor deficits in the lower limbs
Answer: (C) Perineal pain relieved by sitting on a toilet seat
Question 132:
Which of the following findings best differentiates posterior interosseous nerve (PIN) syndrome from a proximal radial neuropathy?
Wrist drop and sensory loss over the dorsum of the hand
Isolated finger and thumb extension weakness without sensory loss
Triceps weakness with diminished reflexes
Numbness in the lateral forearm and palm
Answer: (B) Isolated finger and thumb extension weakness without sensory
Question 133:
Which of the following findings is most consistent with S1 radiculopathy?
Diminished patellar reflex and quadriceps weakness
Diminished ankle reflex and weakness of plantar flexion
Sensory loss over the anterior thigh and weakness of hip flexion
Weakness of dorsiflexion with preserved reflexes
Answer: (B) Diminished ankle reflex and weakness of plantar flexion
Question 134:
Which of the following features most reliably distinguishes Ramsay Hunt syndrome from Bell’s palsy?
Sudden-onset peripheral facial weakness
Loss of taste in the anterior two-thirds of the tongue
Vesicular eruption in the external auditory canal
Hyperacusis on the affected side
Answer: (C) Vesicular eruption in the external auditory canal
Question 135:
Which of the following clinical features is most characteristic of restless legs syndrome?
Muscle weakness during exertion
Sensory loss in a stocking-glove pattern
Discomfort that worsens with rest and improves with movement
Dermatomal pain radiating down the leg
Answer: (C) Discomfort that worsens with rest and improves with movement
Question 136:
Which of the following features most reliably distinguishes reversible cerebral vasoconstriction syndrome (RCVS) from primary angiitis of the CNS (PACNS)?
Presence of thunderclap headache
Multifocal segmental narrowing of cerebral arteries
Reversibility of angiographic abnormalities within 12 weeks
Occurrence of ischemic stroke
Answer: (C) Reversibility of angiographic abnormalities within 12 weeks
Question 137:
Which of the following is the most common neurological manifestation of neurosarcoidosis?
Optic neuritis
Facial nerve palsy
Myelopathy
Hypothalamic dysfunction
Answer: (B) Facial nerve palsy Cranial neuropathies, particularly facial nerve palsy is common in neurosarcoidosis.
Question 138:
Which of the following clinical features best distinguishes serotonin syndrome from neuroleptic malignant syndrome?
Hyperthermia
Altered mental status
Clonus and hyperreflexia
Elevated creatine kinase
Answer: (C) Clonus and hyperreflexia These features are characteristic of Serotonin Syndrome
Question 139:
Which of the following neurological manifestations is most characteristic of Sjögren’s syndrome?
Distal symmetric demyelinating polyneuropathy
Sensory neuronopathy due to dorsal root ganglion involvement
Acute inflammatory demyelinating polyradiculoneuropathy (AIDP)
Lambert-Eaton myasthenic syndrome
Answer: (B) Sensory neuronopathy due to dorsal root ganglion involvement
Question 140:
Which of the following findings is most characteristic of small fiber neuropathy?
Absent vibration sense with reduced nerve conduction velocity
Reduced intraepidermal nerve fiber density with normal nerve conduction studies
Fasciculations and distal weakness with muscle atrophy
Abnormal proprioception and positive Romberg sign
Answer: (B) Reduced intraepidermal nerve fiber density with normal NCS
Question 141:
Which of the following findings is most characteristic of myelomeningocele in spina bifida?
Presence of a CSF-filled sac without neurological deficits
Vertebral arch defect with meninges and spinal cord protrusion
Isolated vertebral defect with a tuft of hair and no symptoms
Fat-containing mass overlying the spine without involvement of neural tissue
Answer: (B) Vertebral arch defect with meninges and spinal cord
Question 142:
Which of the following is a characteristic feature of spinal shock?
Spastic paralysis with hyperreflexia below the lesion
Flaccid paralysis with areflexia below the lesion
Autonomic dysreflexia with severe hypertension
Loss of consciousness and brainstem reflexes
Answer: (B) Flaccid paralysis with areflexia below the lesion
Question 143:
Which of the following genetic changes is most commonly associated with spinal muscular atrophy?
Deletion of the dystrophin gene on Xp21
Mutation in the SMN1 gene on chromosome 5q13
Expansion of CTG repeats in the DMPK gene
Mutation in the RYR1 gene on chromosome 19
Answer: (B) Mutation in the SMN1 gene on chromosome 5q13
Question 144:
Which of the following findings is most characteristic of Stiff Person Syndrome?
Rapidly progressive distal muscle weakness with fasciculations
Continuous motor unit firing relieved by GABAergic therapy
Recurrent demyelinating lesions on MRI
Muscle fiber necrosis with lymphocytic infiltration
Answer: (B) Continuous motor unit firing relieved by GABAergic therapy
Question 145:
Which of the following findings is most suggestive of a cardioembolic source of stroke?
Progressive neurological deficits over several hours
Lacunar infarcts in the basal ganglia
Simultaneous infarcts in multiple vascular territories
Stroke preceded by transient monocular blindness
Answer: (C) Simultaneous infarcts in multiple vascular territories
Question 146:
s Question: Which of the following is the most common cause of spontaneous intracerebral hemorrhage?
Cerebral amyloid angiopathy
Hypertensive small vessel disease
Arteriovenous malformation
Cerebral venous thrombosis
Answer: (B) Hypertensive small vessel disease
Question 147:
oindent Which of the following is the most appropriate next step for a patient presenting with a large vessel occlusion within 6 hours of symptom onset and no contraindications?
Administer high-dose steroids
Begin dual antiplatelet therapy immediately
Proceed with mechanical thrombectomy
Delay intervention until MRI confirms infarct size
Answer: (C) Proceed with mechanical thrombectomy
Question 148:
Which of the following clinical features most strongly suggests a lacunar stroke rather than a large vessel cortical stroke?
Global aphasia and right hemiparesis
Homonymous hemianopia and neglect
Pure motor hemiparesis without cortical signs
Sudden visual loss with retinal artery occlusion
Answer: (C) Pure motor hemiparesis without cortical signs.
Question 149:
Which of the following is the most sensitive investigation for detecting subarachnoid hemorrhage when CT scan is negative and suspicion remains high?
Magnetic resonance imaging (MRI) of the brain
Lumbar puncture demonstrating xanthochromia
CT angiography
Electroencephalography (EEG)
Answer: (B) Lumbar puncture demonstrating xanthochromia.
Question 150:
Which of the following best describes the typical CT appearance of a subdural hemorrhage?
Lentiform (biconvex) hematoma crossing dural reflections
Crescent-shaped hematoma crossing suture lines
Round, focal hyperdensity confined by sutures
Intraventricular hyperdensity after trauma
Answer: (B) Crescent-shaped hematoma crossing suture lines
Question 151:
Which of the following findings is most suggestive of suprascapular nerve entrapment at the spinoglenoid notch?
Weakness of shoulder abduction and external rotation
Isolated infraspinatus weakness with preserved supraspinatus
strength
Loss of sensation over the lateral shoulder
Global atrophy of all rotator cuff muscles
Answer: (B) Isolated infraspinatus weakness with preserved supraspinatus
Question 152:
Which of the following findings is most characteristic of syringomyelia?
Loss of vibration and position sense in a stocking-glove distribution
Dissociated sensory loss with preserved dorsal column modalities
Rapid onset flaccid paralysis of all four limbs
Cranial nerve involvement with ophthalmoplegia
Answer: (B) Dissociated sensory loss with preserved dorsal column sensation
Question 153:
Which of the following best explains the pathophysiology of tardive dyskinesia?
Loss of dopaminergic neurons in the substantia nigra
Upregulation and hypersensitivity of D\(_2\) receptors in the basal ganglia
Autoimmune-mediated basal ganglia destruction
Increased serotonin receptor density in the frontal cortex
Answer: (B) Upregulation and hypersensitivity of D\(_2\) receptors in the basal ganglia
Question 154:
Which of the following physical examination findings is most characteristic of tarsal tunnel syndrome?
Pain with resisted plantar flexion of the ankle
Positive Tinel’s sign posterior to the medial malleolus
Calf tenderness with dorsiflexion of the foot
Pain over the plantar fascia with first-step activity
Answer: (B) Positive Tinel’s sign posterior to the medial malleolus
Question 155:
Which of the following features is most characteristic of giant cell arteritis?
Necrotizing vasculitis involving medium-sized muscular arteries
Granulomatous inflammation with multinucleated giant cells and disruption of the internal elastic lamina
Immune complex deposition in glomerular capillaries
Antineutrophil cytoplasmic antibody (ANCA) positivity
Answer: (B) Granulomatous inflammation with multinucleated giant cells and disruption of the internal elastic lamina.
Question 156:
Which of the following clinical findings is most characteristic of temporomandibular joint syndrome?
Unilateral facial numbness
Jaw deviation with clicking during mouth opening
Pulsatile preauricular bruit
Severe otalgia with tympanic membrane erythema
Answer: (B) Jaw deviation with clicking during mouth opening TMJ
Question 157:
Which of the following clinical findings is most suggestive of neurogenic thoracic outlet syndrome?
Limb cyanosis and venous distension
Digital ischemia and diminished distal pulses
Weakness of intrinsic hand muscles with ulnar sensory loss
Sudden onset of arm swelling following exertion
Answer: (C) Weakness of intrinsic hand muscles with ulnar sensory loss
Question 158:
Which of the following clinical features best distinguishes tics from other movement disorders?
Rhythmic, repetitive, and non-suppressible nature of movements
Sudden, suppressible movements preceded by an urge
Continuous, flowing movements without premonitory sensation
Occurrence only during sleep
Answer: (B) Sudden, suppressible movements preceded by an urge
Question 159:
Which of the following findings most strongly suggests a vascular cause of tinnitus?
High-pitched ringing that is worse in quiet environments
Unilateral tinnitus with associated hearing loss
Pulsatile tinnitus synchronous with the heartbeat
Intermittent tinnitus associated with vertigo
Answer: (C) Pulsatile tinnitus synchronous with the heartbeat.
Question 160:
Which of the following findings most strongly supports the diagnosis of Tolosa-Hunt Syndrome?
Bilateral proptosis with optic disc edema
Rapid resolution of painful ophthalmoplegia with corticosteroid therapy
Slowly progressive ophthalmoplegia with systemic features
Cranial nerve involvement associated with high-grade fever and leukocytosis
Answer: (B) Rapid resolution of painful ophthalmoplegia with corticosteroid therapy
Question 161:
Which of the following is most characteristic of Tourette syndrome?
Presence of motor tics for less than one year
Onset after 21 years of age
Multiple motor and at least one vocal tic lasting for more than one year
Progressive weakness and spasticity
Answer: (C) Multiple motor and at least one vocal tic lasting for more than one year
Question 162:
Which of the following statements regarding TIA is most accurate?
Symptoms must resolve within 6 hours to qualify as a TIA
Evidence of acute infarction on MRI excludes the diagnosis of TI
TIAs rarely precede ischemic strokes.
Cardioembolic sources are less common than small-vessel disease in
Answer: (D)
Question 163:
Which of the following findings most strongly suggests neuromyelitis optica spectrum disorder rather than idiopathic transverse myelitis?
A lesion involving fewer than two vertebral segments
Presence of oligoclonal bands in CSF
Positive aquaporin-4 (AQP4) antibodies
Rapid recovery without immunotherapy
Answer: (C) Positive aquaporin-4 (AQP4) antibodies
Question 164:
Which of the following features most strongly suggests secondary rather than classical trigeminal neuralgia?
Unilateral, electric shock-like pain triggered by touch
Pain limited to V2 and V3 divisions
Presence of facial numbness between attacks
Good response to carbamazepine
Answer: (C) Presence of facial numbness between attacks
Question 165:
Which clinical feature most reliably distinguishes trochlear nerve palsy from skew deviation?
Diplopia worse on downgaze
Compensatory head tilt
Torsional deviation toward excyclotorsion
Increased hypertropia with head tilt toward the affected side
Answer: (D) Increased hypertropia with head tilt toward the affected side
Question 166:
A 39-year-old male with a history of pulmonary tuberculosis presents with seizures. MRI of the brain shows a ring-enhancing lesion in the left motor cortex with a hypointense center and hyperintense rim. MR spectroscopy demonstrates a prominent lipid-lactate peak and reduced N-acetylaspartate (NAA) levels. Which of the following diagnostic findings most strongly supports tuberculoma over other ring-enhancing lesions?
Presence of restricted diffusion
Detection of Mycobacterium tuberculosis DNA by PCR in cerebrospinal fluid
Visualization of a scolex within the cystic lesion on MRI
Elevated choline-to-creatine ratio
Answer: (B) Detection of Mycobacterium tuberculosis DNA by PCR in cerebrospinal fluid. Restricted diffusion favors abscess, elevated choline-to-creatine suggest malignancy and scolex in cystic lesion suggests neurocysticercosis.
Question 167:
Which of the following is the most effective diagnostic test for confirming ulnar neuropathy at the wrist?
MRI
Ultrasound
Nerve conduction studies (NCS)
Xray
Answer: (C) Nerve conduction studies (NCS)
Question 168:
Which of the following findings most strongly supports a diagnosis of primary CNS vasculitis?
Sudden-onset focal neurological deficits with a normal MRI
Multifocal cerebral infarcts of varying ages with negative systemic vasculitis workup
Isolated posterior circulation stroke with atrial fibrillation
Symmetric periventricular white matter hyperintensities without infarction
Answer: (B) Multifocal cerebral infarcts of varying ages with negative systemic vasculitis workup
Question 169:
Which of the following features is most characteristic of vascular dementia compared to Alzheimer’s disease?
Early episodic memory impairment
Stepwise cognitive decline following cerebrovascular events
Visual hallucinations
Rapidly progressive aphasia
Answer: (B) Stepwise cognitive decline following cerebrovascular events
Question 170:
Which of the following is considered the gold standard for confirming the diagnosis of vasculitic neuropathy?
Electromyography
MRI of peripheral nerves
Nerve biopsy
Blood tests
Answer: (C) Nerve biopsy is the gold standard, demonstrating vessel wall inflammation
Question 171:
Which of the following findings is most characteristic of benign paroxysmal positional vertigo (BPPV)?
Continuous vertigo with hearing loss
Episodic vertigo triggered by head position changes
Vertigo with focal neurological deficits
Vertigo associated with visual aura and photophobia
Answer: (B) Episodic vertigo triggered by head position changes
Question 172:
Which artery is most commonly implicated in Wallenberg Syndrome?
Basilar artery
Anterior inferior cerebellar artery
Posterior inferior cerebellar artery
Superior cerebellar artery
Answer: (C) Posterior inferior cerebellar artery
Question 173:
Which of the following is not part of the classic triad of Wernicke’s encephalopathy?
Confusion
Ataxia
Ophthalmoplegia
Hyperreflexia
Answer: (D) Hyperreflexia
Question 174:
Which of the following clinical features is least likely to be associated with West Nile Encephalitis?
Fever and altered mental status
Neck stiffness and photophobia
Acute flaccid paralysis
Erythematous maculopapular rash
Answer: (D) Erythematous maculopapular rash — Rash is uncommon in
Question 175:
Which of the following findings is most specific for Wilson’s disease?
Elevated serum ferritin
Low serum ceruloplasmin with Kayser-Fleischer rings
Hyperammonemia and elevated INR
Increased serum alpha-fetoprotein
Answer: (B) Low serum ceruloplasmin with Kayser-Fleischer rings
Question 176:
Which of the following biochemical findings is characteristic of X-linked adrenoleukodystrophy?
Decreased plasmalogen synthesis
Elevated very long-chain fatty acids due to peroxisomal β-oxidation defect
Elevated lysosomal enzyme activity
Reduced branched-chain amino acid levels
Answer: (B) X-linked adrenoleukodystrophy results from defective transport of VLCFAs