Neuro Flashcards

1
Q

In which age group may ‘Kernig’s sign’ not be present in meningitis?

A

Under 18months.
May present as non-specific drowsiness, fever, irritability, poor-feeding.
Kernig’s sign- neck stiffness

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2
Q

When is a lumbar puncture contraindicated??

A
Prolonged or focal seizure 
Focal neurology
Purpuric rash
Gcs<13
Abnormal pupils or posture
Coagulation disorder 
Cushings triad (low hr, high bp, irregular resp)
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3
Q

What is the appropriate step wise management for status epilepticus?

A

1) buccal medazolam/ iv lorazepam
2) Iv lorazepam
3) iv phenytoin (iv phenobarbital if on Reg phenytoin)
4) rapid sequence control using general anaesthetic using thiopental sodium

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4
Q

What symptoms would you get if the cerebellar was affected?

A

Tremors
Mystsgmus
Gait instsbility
Speech difficulty

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5
Q

Hyperventilation can trigger what type of seizures ?

A

Absence epilepsy

Rx- ethosuximide
If associated with other seizure types give sodium valprorate

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6
Q

What is the commonest neuromuscular disease/dystrophy?

A

Dystrophinopathy (duchennes muscular dystrophy) 1/3500 live boys

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7
Q

What disease modifying agent can be give in duchenne muscular dystrophy?

A

Glucocorticoids

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8
Q

What is Charcot-Marie-tooth disease?

A

AD demyelinating peripherals neuropathy (pmp22 gene)

Leads to distal weakness and atrophy and sensory loss.

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9
Q

What is spinal muscular atrophy?

A

Disorder of the SMN1 gene. Low levels in the anterior horn of the spinal cord leads to loss of function and muscle wasting.

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10
Q

What causes a floppy baby?

A

Cerebral

  • IVH, hydrocephalus
  • structural abnormality
  • chromosomal disorders
  • perxisomal

Peripheral

  • anterior horn cell (SMA)
  • demyelination -
  • axonal neuropathy
  • myasthenia syndromes
  • congenital muscle disease (dystrophy, myopathy, myotonic dystrophy)
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11
Q

What is tuberous sclerosis?

A

Neuro-cutaneous disease
Depigmented ‘ash leaf’ spots, rough skin on lumbar spine,
Development delay, epilespsy, intellectual impairment

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12
Q

What is Rolandic epilepsy?

A

Infrequent partial fits. Unilateral or oropharyngeal sensory motor symptoms. Speech arrest. Hypersalivation

Rx rarely needed, sulthiame sometimes uses.

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13
Q

Causes of meningitis in neonates?

A

Group b strep
Listers
E. Coli

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14
Q

Treatment for meningitis?

A

Ceftriaxone

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15
Q

What is seen on eeg in west syndrome epilepsy?

A

Hypsarrthyimia - chaotic pattern, slow sharp waveforms.

Age 4-6months
Salaam attacks (on waking), low Iq
Rx : vigabatrin

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16
Q

What is seen on eeg in Ohtahara syndrome?

A

Supppression- burst pattern

Rx - chloralhydrate
Onset <3months

17
Q

What is Lennox-gastaut syndrome?

A

Extension of infantile spasms.
Handicapped (90%) poor prognosis

Eeg : slow spike

Rx- ketogenic diet might help

18
Q

What is rolandic epilepsy?

A

Benign, brief partial fits often unilateral facial or oropharyngeal sensory motor symptoms (hyper salivation)
Rx - sulthiame

19
Q

Types of cerebral palsy?

A

70% - spastic (UMN injury)

Dyskinetic - basal ganglia (involuntary uncontrolled movements)

Ataxic - cerebellum damage

Mixed

20
Q

Causes of cerebral palsy?

A

Pre birth - 80% - toxo, cmv, rubella. Cerebral malformation

Birth - birth asphyxiation, trauma

Post natal - intra ventricular haemorrhage, meningitis, head trauma, kernicterus

21
Q

What is the prognosis for someone with retinoblastoma ?

A

Many visually impaired

Risk of cancer - sarcoma

22
Q

What is a cephalhaematoma?

A

Lump from ruptured vessels between skull and periosteum.

Causes prolonged second stage of labour and instrumental delivery

23
Q

What is the difference in presentation for caput succedaneum and cephalhamatoma?

A

CS - extraperiosteal and crosses the suture lines. Resolves few days.

CH- does not cross suture lines. Resolves few months.