Clinical Flashcards

1
Q

Rhabdomyolysis after exertion, fasting or in association with a viral illness raises the suspicion for what group of disorders?

A

Metabolic myopathies

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2
Q

Strength and CK levels of metabolic myopathies

A

Normal inbetween episodes

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3
Q

What is the most common metabolic cause of repeated myoglobinuria?

A

CTPII deficiency

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4
Q

Myoadenylate deaminase deficiency shows what on ischemic exercise testing?

A

Failure to generate ammonia

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5
Q

What is the most proximal abnormal posterior interosseous innervated muscle possible?

A

Extensor digitorum communis (C7-C8)

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6
Q

What cervical nerve roots are most commonly affect in cervical radiculopathy?

A
  • C7 (1st)
  • C6 (2nd)
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7
Q

What is the most common form of CMT peripheral neuropathy?

A

CMT 1A: duplication of chromosome 17p11.2-12 region containing the peripheral myelin protein 22 gene

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8
Q

What are the limitations in Erb’s palsy and where is the potential lesion?

A
  • Trouble supinating forearm, extending wrist, flexing elbow, abducting shoulder and externally rotating shoulder
  • Traction injury to the upper trunk or C5/C6 nerve roots
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9
Q

What are the 3 levels of nerve injury from least to worst?

A
  1. Neuropraxia: (mild)
    1. Disruption of the myelin shealth (conduction block)
    2. No Wallerian degeneration
    3. Conduction block causes Sensory loss
  2. Axonotmesis: (moderate)
    1. Demyelination causes axonal damage
    2. Wallerian degeneration
    3. Endoneurium and schwann cells intact
    4. Motor and sensory loss
  3. Neurotmesis
    1. Complete loss of axon, schwann cells and endoneurium
    2. Complete motor and sensory loss
    3. No spontaneous recovery
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10
Q

What percent of patients with MGUS will go on to develop a malignant plasma cell dyscrasia?

A

19%

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11
Q

What kind of neuropathy is associated with amyloidosis?

A

Small fiber neuropathy

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12
Q

What monoclonal protein is usually seen with amyloidosis?

A

IgG or IgA

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