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Core Concepts

Neurology focuses on diseases of the central (brain, spinal cord) and peripheral (nerves, muscles, neuromuscular junction) nervous systems. Key to diagnosis is anatomical localisation of lesions and understanding the pathophysiological process. Common presentations include weakness, sensory disturbances, abnormal movements, headaches, seizures, and cognitive impairment. The cranial nerves, sensory tracts (spinothalamic, posterior column), and motor tracts (corticospinal) are fundamental for localisation.

Clinical Presentation

  • Stroke/TIA: Acute onset focal neurological deficit (e.g., hemiparesis, dysphasia, visual field loss). TIA symptoms resolve within 24 hours.
  • Seizures: Transient disturbance of brain function due to abnormal electrical activity. Can be generalised (e.g., tonic-clonic, absence) or focal (with or without impaired awareness).
  • Multiple Sclerosis (MS): Relapsing-remitting episodes of neurological dysfunction (e.g., optic neuritis, sensory symptoms, weakness, ataxia), separated in time and space.
  • Parkinson's Disease: Bradykinesia, rigidity (cogwheel), resting tremor (pill-rolling), postural instability.
  • Myasthenia Gravis: Fluctuating fatigable weakness, worse with exertion, better with rest. Affects ocular muscles (ptosis, diplopia), bulbar muscles (dysphagia, dysarthria), and limbs.
  • Guillain-BarrΓ© Syndrome (GBS): Rapidly progressive, ascending flaccid paralysis with areflexia, often preceded by infection. Risk of respiratory failure.
  • Motor Neuron Disease (MND/ALS): Progressive weakness with signs of both upper (spasticity, brisk reflexes) and lower (fasciculations, wasting) motor neuron involvement, typically without sensory loss.
  • Headaches:
    • Migraine: Unilateral, pulsatile, moderate-severe, photophobia/phonophobia, aura.
    • Tension: Bilateral, band-like, mild-moderate, no severe associated symptoms.
    • Cluster: Unilateral, excruciating periorbital pain, associated with ipsilateral autonomic features (lacrimation, ptosis, rhinorrhoea).
  • Dementia: Progressive decline in memory and other cognitive functions (e.g., language, executive function, visuospatial skills) severe enough to interfere with daily life.

Diagnosis (Gold Standard)

Stroke: Immediate CT brain to rule out haemorrhage. MRI brain (DWI sequence) for acute ischemia. Carotid Doppler for TIA/ischemic stroke workup.
Seizures: Clinical diagnosis, EEG (epileptiform activity), MRI brain to exclude structural lesions.
MS: MRI brain and spinal cord (dissemination in space and time per McDonald criteria), CSF oligoclonal bands.
Parkinson's Disease: Clinical diagnosis based on UK Brain Bank criteria. DAT scan can aid differentiation from essential tremor.
Myasthenia Gravis: Acetylcholine receptor antibodies (most common), MuSK antibodies. EMG (decremental response to repetitive nerve stimulation).
GBS: Clinical criteria, CSF (albumino-cytological dissociation), NCS/EMG (demyelinating features).
MND: Clinical diagnosis (El Escorial criteria), EMG (denervation/reinnervation).
Headaches: Clinical (International Headache Society criteria). MRI for red flags.
Dementia: Clinical history, cognitive screening (MMSE, MoCA), MRI brain (atrophy, vascular changes, rule out reversible causes).

Management (First Line)

Ischemic Stroke: IV thrombolysis (alteplase within 4.5h), mechanical thrombectomy (within 6-24h for large vessel occlusion). Antiplatelets (aspirin), statins, blood pressure control, rehabilitation.
Haemorrhagic Stroke: Blood pressure control, neurosurgical consultation for evacuation in selected cases.
Acute Seizures: IV lorazepam/diazepam. Status epilepticus: IV benzodiazepines, then phenytoin/levetiracetam/valproate. Long-term Seizure: Antiepileptic drugs (e.g., lamotrigine, levetiracetam, carbamazepine, valproate) based on seizure type and patient factors. Parkinson's Disease: Levodopa (most effective), dopamine agonists (e.g., ropinirole), MAO-B inhibitors (e.g., rasagiline). MS Relapse: High-dose IV corticosteroids (methylprednisolone). Disease-modifying therapies (DMTs) for long-term management (e.g., interferon-beta, glatiramer acetate, natalizumab, ocrelizumab). Myasthenia Gravis: Pyridostigmine (symptomatic). Immunosuppression (steroids, azathioprine). Crisis: IVIG or plasmapheresis. GBS: IVIG or plasmapheresis. Supportive care, including respiratory support. MND: Riluzole (slows progression). Symptomatic management (e.g., baclofen for spasticity, non-invasive ventilation). Migraine: Acute: NSAIDs, triptans. Prophylaxis: Beta-blockers (propranolol), topiramate, amitriptyline. Cluster Headache: Acute: High-flow oxygen, sumatriptan SC. Prophylaxis: Verapamil. Alzheimer's Dementia: Cholinesterase inhibitors (donepezil, rivastigmine, galantamine) for mild-moderate. Memantine for moderate-severe.

Exam Red Flags

  • Thunderclap headache: Sudden, severe headache reaching maximal intensity in seconds. Consider Subarachnoid Haemorrhage (SAH) – urgent CT head.
  • Headache with papilloedema: Raised intracranial pressure (e.g., brain tumour, idiopathic intracranial hypertension, cerebral venous thrombosis).
  • Fever, headache, neck stiffness, photophobia: Meningitis/Encephalitis – urgent LP after CT head (if indicated).
  • New-onset focal neurological deficit (acute): Stroke/TIA.
  • Acute painful vision loss in elderly with jaw claudication: Giant Cell Arteritis – urgent ESR/CRP and steroid treatment.
  • New onset seizure in adult: Rule out structural causes (e.g., tumour, stroke) with MRI brain.
  • Progressive weakness with respiratory compromise: Myasthenic crisis, GBS, MND – requires urgent airway assessment.
  • Unexplained gait disturbance, urinary incontinence, dementia: Normal Pressure Hydrocephalus.

Sample Practice Questions

Question 1

A 45-year-old male smoker presents with a history of recurrent, severe headaches. He describes sudden onset, excruciating, unilateral retro-orbital pain occurring several times a day for a few weeks, then disappearing completely for months. Each attack lasts approximately 45 minutes. During the attacks, he notices ipsilateral lacrimation, conjunctival injection, and nasal congestion. He reports feeling restless and needing to pace during these episodes. What is the most likely diagnosis?

A) Migraine with aura
B) Tension-type headache
C) Trigeminal neuralgia
D) Cluster headache
Explanation: This area is hidden for preview users.
Question 2

A 72-year-old woman develops sudden onset of 'the worst headache of her life', accompanied by neck stiffness, photophobia, and nausea. She has no focal neurological deficits. Her blood pressure is 160/90 mmHg. What is the most appropriate diagnostic investigation?

A) CT Angiography of the brain
B) Lumbar Puncture
C) Non-contrast CT head
D) EEG
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Question 3

A 58-year-old woman presents with gradually progressive difficulty walking over the past year. She describes stiffness and slowness of movement, and her family has noticed a reduced facial expression and a tremor in her right hand at rest. On examination, she has a stooped posture, bradykinesia, cogwheel rigidity, and a resting tremor. Her cognition is intact. What is the most likely diagnosis?

A) Essential Tremor
B) Multiple Sclerosis
C) Parkinson's Disease
D) Huntington's Disease
Explanation: This area is hidden for preview users.

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