16 - Neuro Flashcards

1
Q

CN I:

A

Olfaction / smell

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2
Q

CN II:

A

Vision - newborns 20/200, by 6mos 20/20

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3
Q

Features of Horner syndrome

A

Interruption of sympathetic innervation to the pupil

  1. Ptosis
  2. Miosis
  3. Facial anhydrosis
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4
Q

Rooting reflex is associated with which cranial nerve?

A

V (trigeminal)

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5
Q

What is Gower sign?

A

Patient arises from lying on floor by using arms to “climb up” legs and body

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6
Q

Lower motor neuron lesions and cerebellar lesions result in muscle tone increase or decrease?

A

Decrease (hypotonia)

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7
Q

Upper motor neuron lesions result in muscle tone increase or decrease?

A

Increase (hypertonia or spasticity)

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8
Q

What is the MC recurrent pattern of primary HA’s in children and adolescents?

A

Tension HA

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9
Q

Triptans are contraindicated for:

A

Focal neuro deficits with migraines or basilar migraines (syncope) -> stroke risk

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10
Q

Who gets migraine prophylaxis?

A

> 1 disabling migraine per week

BB’s (propanolol)(CI: asthmatics and DM)

TCA’s

Anti-convulsants

CCB’s

SSRI’s

Antihistamines

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11
Q

Jacksonian march?

A

Complex partial seizure spreading from face to arm to leg

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12
Q

Txt for absence seizures?

A

Ethosuximide or valproic acid

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13
Q

Stat-ep

A

> 30mins

Causes: new-onset epilepsy, drug intox or withdrawal, electrolytes, hypoxia, stroke, head trauma

Lorazepam, diazepam, midazolam

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14
Q

MCC of seizure between 6mo and 6yrs?

A

Febrile seizure

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15
Q

What is spinal muscular atrophy?

A

SMA

Progressive anterior horn cell degeneration

“Floppiness”

Absent DTR’s

Tongue fasciculations

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16
Q

Where is polio endemic?

A

Nigeria
India
Pakistan
Afghanistan

17
Q

MCC of acute flaccid paralysis in children?

A

Guillain Barre syndrome

Postinfectious autoimmune peripheral neuropathy

Symmetrical ascending weakness over hours to weeks

Cam affect respiratory function

Slow spontaneous resolution

Tx: IVIG, plasma exchange, immunosuppresive drugs

18
Q

Charcot-Marie-Tooth dz

A

Ankle-weakness, frequent tripping, pes cavus

Slow progression

No txt

19
Q

What are the three types of childhood myasthenia gravis?

A

Juvenile myasthenia gravis

Transient neonatal myasthenia gravis

Congenital myasthenia gravis (not AI - genetic mutations)

20
Q

Txt for MG?

A

Acetylcholinesterase inhibitor (pyridostigmine)

Thymectomy (reduced antibody burden)

Steroids

21
Q

Seizures and concussion?

A

At time of injury - ok

Within 7 days - ok

After seven days - can lead to epilepsy (glial scarring)

22
Q

Sxs for concussion last how long?

A

Less than 3 days

Most resolve within a week

23
Q

Return to play after concussion

A
  1. Rest
  2. Walking
  3. Sport-specific exercise
  4. Non-contact resistance training
  5. Full-contact
  6. Game play

Q24h step-up

24
Q

Epidural hemorrhage

A

Onset minutes to hours
Lucid interval followed by progressive neuro deficits

Lens-shaped extra-cerebral hemorrhage compressing the brain

Txt - surgical evactuation

25
Subdural hemorrhage
Onset over hours Focal neuro deficits Crescentic shape on CT Surgical evacuation
26
Subarachnoid hemorrhage
Worst headache of my life Stiff neck Supportive care
27
Neurofibromatosis Type 1
Neurofibromas composed of schwann cells Cafe au lait spots Axillary or inguinal freckling Iris hamartomas (Lisch nodules) Malignancy risk Learning disabilities, scoliosis, seizures - reduced life-span (10-15yrs)
28
Cardinal features of tuberous sclerosis?
Facial angiofibromas (adenoma sebaceum) MR Epilepsy
29
Ash leaf spots and Shagreen patches, think:
Tuberous sclerosis