Neurology Flashcards

1
Q

What are the signs of a migraine?

A
Hemi-cranial pain
Throbbing
Relieved by rest
Photophobia 
Phonophobia
Younger – abdominal pain, nausea, vomiting
Older – aura (visual, sensory, motor)
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2
Q

How are migraines treated?

A

Acute attack – pain relief, triptans

Preventative if 1 or more per week – propranolol, pizotifen

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3
Q

What are the symptoms of tension-type headaches?

A

Symmetrical
Band-like distribution
Present most of the time
Constant ache

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4
Q

How are tension-type headaches treated?

A

Reassurance
Acute attacks – analgesia
Prevention – amitriptyline

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5
Q

What are the causes of epilepsy?

A
None
Infection
Hyponatraemia
Toxins
Trauma
Tumour
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6
Q

What are the 2 main types of seizures?

A

Partial/focal - affects 1 hemisphere

Generalised - affects 2 hemispheres

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7
Q

How is epilepsy investigated?

A
History
Video recording
ECG in convulsive seizures
EEG – if + clinical diagnosis
MRI
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8
Q

How is epilepsy treated?

A
Partial/focal – carbamazepine 
Generalised – sodium valproate (not in girls)
Lamotrigine
Other – steroids, immunoglobulins
Vagus nerve stimulation
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9
Q

What are the side effects of anti-epileptics?

A

Drowsiness

Can affect learning, cognition and behaviour

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10
Q

What are the signs of a febrile convulsion?

A

Rapid temperature rise
Simple – generalised tonic clonic, <15mins, only occur once in a single febrile illness
Complex – partial or focal seizures, >15mins, occur multiple times during the same febrile illness

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11
Q

What age group does febrile convulsions affect?

A

6 months - 5 years

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12
Q

What are the causes of febrile convulsions?

A

Fever caused by an underlying viral illness or bacterial infection

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13
Q

How are febrile convulsions treated?

A

Analgesia

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14
Q

How is duchenne muscular dystrophy inherited?

A

X-linked recessive

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15
Q

What gene is defective in duchenne muscular dystrophy?

A

Defective gene for dystrophin on the X chromosome

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16
Q

What are the signs of duchenne muscular dystrophy?

A

Symmetrical proximal weakness – waddling gait, calf hypertrophy, gower’s sign
Delayed gross motor signs
Cardiomyopathy

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17
Q

What is Gower’s sign?

A

In duchenne muscular dystrophy

Children with proximal muscle weakness use a specific technique to stand up from lying

18
Q

How is duchenne muscular dystrophy treated?

A
No curative treatment
Occupational therapy
Physiotherapy
Oral steroids
Creatine supplement
19
Q

What are signs of raised intracranial pressure?

A

Headache aggravated by coughing, staining at stool, bending etc
Woken from sleep with headache +/- vomiting

20
Q

What are indications for neuroimaging with regards to headaches?

A
Features of cerebellar dysfunction
Features of raised intracranial pressure
New focal neurological deficit – eg new squint
Seizures – especially focal
Personality change
Unexplained deterioration of schoolwork
21
Q

What is a seizure fit?

A

Any sudden attack from whatever cause

22
Q

What is syncope?

A

Faint - neuro-cardiogenic mechanism

23
Q

What is a convulsion?

A

Seizure where there is prominent motor activity

24
Q

What is an epileptic seizure?

A

An electrical phenomenon

25
Q

What are other kinds of non-epileptic seizures?

A

Reflex anoxic seizure
Parasomnia
Psychogenic non-epileptic seizures

26
Q

When should you measure a child’s head?

A
Every time you see them between birth and 3 years or any child with neurological symptoms
Occipitofrontal circumference (OFC)
27
Q

Microcephaly

A

Mild – OFC <2 SD
Moderate/severe – OFC <3 SD
Normally indicates small brain (microencephaly)
Has it always been a small head or is it not growing?
Causes – antenatal, postnatal, genetic and environmental

28
Q

Macrocephaly

A

OCF >2 SD
Can only grow if the sutures are still open
Large brain? Development?
Other physical abnormalities – facial features, hepatosplenomegaly, bony deformities etc

29
Q

Plagiocephaly

A

Flat head, squint

Ears at different levels

30
Q

Brachycephaly

A

Short head or flat at the back

Down syndrome

31
Q

Scaphocephaly

A

Boat shaped skull

32
Q

Craniosynostosis

A

Cranial sutures close too early impairing bone growth

Needs to be corrected within 1 year

33
Q

Deformational plagiocephaly

A

Reflects the in-utero position of the baby

34
Q

When would you suspect a neuromuscular disorder in a child?

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
35
Q

What is the pathology of cerebral palsy?

A

Disorder of movement and posture

Associated with a fixed insult to the developing brain

36
Q

What are the causes of cerebral palsy?

A
Pre-natal, peri-natal, post-natal:
Ischaemia
Congenital infection
Neonatal meningitis
Prematurity
Kernicterus
37
Q

What are the symptoms of cerebral palsy?

A

Spastic – increased tone/reflexes, reduced power
Dystonic – involuntary movements
Ataxic – hypotonia, wide-based gait, nystagmus, intention tremor

38
Q

What investigations would be done if cerebral palsy was suspected?

A

Creatinine kinase - increased

CT/MRI

39
Q

How is cerebral palsy treated?

A

MDT

40
Q

What are causes of neonatal seizures?

A
Hypoxic-ischaemia encephalopathy
Infection – meningitis/encephalitis
Intracranial haemorrhage/infarction
Structural CNS lesions
Metabolic disturbance – hypoglycaemia
Metabolic disorders 
Neonatal withdrawal from maternal drugs or substance abuse
Kernicterus