Neurology 4 Flashcards

1
Q

Musculocutaneous nerve function?
Motor
Sensory

A

Motor = Elbow flexion

Sensory = lateral part of FOREARM

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2
Q

Flexion weakness at elbow - what nerve affected

Flexion weakness at wrist - what nerve affected

Flexion weakness at fingers - what nerve affected

Extension of elbow/wrist/fingers - what nerve affected?

A
Elbow = Musculocutaneous
Wrist = Median
Fingers = Median/ulnar

Extension weakness = Radial

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3
Q

Median motor function?

A

Flexion of wrist and fingers ( except medial 2 fingers - Ulnar)

LOAF muscles
Lateral 2 lumbricals
Opponens pollicis brevis
Abductor pollicis brevis
Flexor pollicis brevis
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4
Q

Ulnar nerve function

A

Finger abduction and adduction

Flexion of 4,5th digit = Flexor digitorum profundus

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5
Q

Axillary nerve function?

A

Shoulder abduction

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6
Q

Erb palsy - waiter’s tip lesion where and presentation?

A

C5-6 lesion
Loss of elbow flexion and shoulder movement
Sensory loss in lateral aspect of arm

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7
Q

Klumpke palsy - lesion where and presentation?

A

C8 - T1 lesion

Supinated clawed hand + hyperextension at wrist

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8
Q

Flaccid foot + Knee flexion = only 1 nerve cause this - name?

A

Sciatic nerve

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9
Q

Once wallerian degeneration completes - denervated dying motor axon fibers express what?

A

Acetycholine - so inappropriate firing of motor in response to Ach = sign of denervation

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10
Q

Neurogenic changes

morphology and recruitment of muscle unit action potential

A

surviving motor axons - tries to re-innervate died motor
-fibers = thin and unmyelinated
Longer/Broad/Polyphasic/ high amplitude!

Reduced recruitment!

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11
Q

Myopathic changes

morphology and recruitment of muscle unit action potential

A

muscle fibers damaged + few remaining ( but are normal)

Small amplitude + normal/increased recruitment+ early

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12
Q

AChr antibodies a/w what?

A

Thymoma and thymic hyperplasia

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13
Q

Musk antibodies a/w what?

A

Generalized severe MG ( bulbar and respiratory involvement)

-young female - non white

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14
Q

Singe fibre EMG best for?

A

Ocular MG

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15
Q

Medications to avoid in MG?

A
Aminoglycosides
Tetracyclines
Macrolides
Fluoroquinolones
B-blockers
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16
Q

Lambert-eaton syndrome?

A

Triad of ;
1 - proximal weakness (upper limbs most affected) - mild improvement post exercise
2- autonomic features - dry mouth/erectile dysfunction/urinary issues
3- areflexia ( post exercise)

NO SENSORY/ NO FATIGUABILITY

17
Q

Lambert-eaton syndrome a/w?

A

Paraneoplastic - SCLC

Non-paraneoplastic - HLA B8 DR3

18
Q

Lambert-eaton treatment?

A

Resect tumor

3-4 diaminopyridine - block K from going out - prolonged depolarisation

19
Q

Antibodies a/w Dermatomyositis and ILD?

Malignancy in ILD patients?

what Dermatomyositis antibodies associated with good response to treatment?

A

anti-MDA5 - rapidly progressive ILD
Anti-Jo 1 - ILD

Lower risk

Anti-MI 2

20
Q

Treatment for dermatomyositis?

A

Prednisolone (iv methylprednisolone if severe weakness)

CYP if ILD

21
Q

SLCO1B1 gene function?

A

uptake of statin into liver cells

22
Q

Necrotizing autoimmune myopathy antibodies?

A

anti-SRP/anti-HMG COA

high CK

23
Q

Anti-SRP a/w?

A

Dilated cardiomyopathy

No response to immunosuppression

24
Q

Anto-HMG COA a/w?

A

higher levels of CK and muscle weakness severity
HIGHLY SPECIFIC FOR NECROTIZING AUTOIMMUNE MYOPATHY
-can occur without statins

25
Q

Signal recognition particle is what?

A

Peptide involved in transport protein to endoplasmic reticulum

26
Q

Commonest myopathy > 50 yrs old?

A

Inclusion body myositis ( distal + asymmetric weakness)

27
Q

what muscle is spared in IBM quadriceps weakness?

A

Rectus femoris

All the vastus muscle affected-atrophy

28
Q

Perimysial,endomysial inflammation and necrosis - have upregulation of what?

A

MHC1 - CD8 complex

29
Q

Anti-synthetase syndrome is what?

A
Myositis with;
ILD
Mechanic hands and polyarthritis
Fever
Raynaud's
30
Q

Myopathy in ;
Hypothyroidism features?

Hyperthyroidism features?

A
  • Symmetric PAINFUL muscle cramps, weakness
  • occasional HIGH CK
  • Delayed reflexes
  • PAINLESS muscle weakness
  • NORMAL CK
  • brisk reflexes
31
Q

Statin induced NAM - HLA antibodies
protective?
at risk?
association with SLCO1B1 gene?

A

At risk - HLA DRB1 11

Protective - HLA DQA1/ DQB6

No! SLCO1B1 only for Statin myopathy