neurology Flashcards

1
Q

common problems

A
migraine
traumatic brain injury
tourette syndrome
epilepsy
brain tumour
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2
Q

headache

A

chronic progressive
chronic non progressive
growth is very important to access
not growing well- congenital brain tumour (craniopharyngioma)
common causes of secondary headache- sinuses

differentiate primary/secondary

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3
Q

Pointers to child hood migraine

A
abdo pain, nausea, vomiting
focal symptoms/ signs, during after attack
Aura, aggravated by bright light and sound
family history positive
relation to fatigue / stress
Hemicranial pain
Throbbing/ pulsatile
Abdo pain, nausea, vomiting
Relieved by rest
Photophobia/ phonophobia
Visual, sensory, motor aura
Positive family history
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4
Q

tension headache

A

symptomless, present all the time.

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5
Q

Management

A

Acute attack: effective pian relief, triptans

Preventative (at least 1/week): Pizotifen, Propranolol, Amitryptyline, Topiramate, Valproate

more than one migraine a week
preventive treatment.

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6
Q

syncope

A

Faint (a neuro-cardiogenic mechanism)

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7
Q

Epileptic seizure

A

abnormal hypersynchronous discharge from a group of neurons mainly your cortex

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8
Q

Febrile seizures

A

read more

An seizure occurring in infancy/ childhood, usually between 3 months and 5 years of age, associated with fever but without evidence of intracranial infection or defined cause for the seizure
Commonest cause of ‘acute symptomatic seizure’ in childhood

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9
Q

seizure type

A

Fall: Atonic/ tonic/ myoclonic

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10
Q

infantile spams

A

6months to 12 months

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11
Q

tonic clonic seizures

A

eyes are open

difficulty breathing

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12
Q

provoked seizure

A

environmental stimulus overstimulates vagus nerve

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13
Q

diagnosis

A

History
Video recording of event
ECG in convulsive seizures
Interictal/ ictal EEG
MRI Brain: to determine etiology eg. Brain malformations/ brain damage
Genetics: idiopathic epilepsies are mostly familial; also single gene disorders eg. Tuberous sclerosis
Metabolic tests: esp if associated with developmental delay/ regression

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14
Q

How fontanelles close

A

two gaps anterior and posterior fontanelle

posterior close in 3 months
anterior close 18 to 22 months

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15
Q

Abnormal head shape

A

Plagiocephaly ‘flat-head’
Brachycephaly ‘short head or flat at back’- down syndrome
Scaphocephaly ‘boat shaped skull’
Craniosynostosis

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16
Q

When to suspect a NM disorder

A
Baby ‘floppy’ from birth
Slips from hands
Paucity of limb movements
Alert, but less motor activity
Delayed motor milestones
Able to walk but frequent falls

Complete head lag

17
Q

Muscular dystrophy

A

CK is raised