Muscle Flashcards

1
Q

fewer, but larger, motor unit action potentials on EMG

A

nerve injury with denervation and reinnervation

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2
Q

In myopathies, the muscle fibers

A

are not atrophic and angular

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3
Q

In myopathies, the number of motor units is

A

not decreased, unlike neurogenic disorders, because the number of motor neurons or axons are normal. The motor unit action potentials are smaller

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4
Q

elevated serum CK

A

may indicate myopathy

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5
Q

X-linked recessive inheritance disease

A

Duchenne Muscular Dystrophy - can cause Necrosis, Atrophy, Segmental fiber over-contraction, Connective tissue proliferation

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6
Q

antisense oligonucleotide that restores the reading frame

A

morpholino - may be future treatment for duchenne’s!

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7
Q

autosomal dominant diseases characterized by weakness and myotonia, they also can have involvement of multiple organs

A

Myotonic dystrophies

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8
Q

Measurement of serum lactate shows the lack of normal increase during exercise

A

McArdle’s Disease -muscle phosphorylase deficiency, can’t break down glycogen

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9
Q

Hyperparathyroidism might present with

A

severe weakness resembling amyotrophic lateral sclerosis

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10
Q

Hypothyroidism patients present with

A

muscle spasms but not weakness, and could have a very high serum creatine kinase levels, so this should be suspected in obese patients with hyperlipidemia and high serum creatine kinase

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11
Q

Myopathies from toxins or medications could be associated with either :

A

muscle fiber atrophy, vacuolization , myofibrillary degeneration , mitochondrial dysfunction, or fiber necrosis.

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12
Q

compound action potential becomes larger during fast stimulation rates

A

presynaptic - Eaton Lambert

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13
Q

amplitude becomes smaller during slow, repetitive stimulation

A

Myasthenia Gravis

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14
Q

treating myasthenia gravis

A

Anticholinesterase drugs such as pyridostigmine
Corticosteroids
Immunosuppressants:
azathioprine, cyclophosphamide, mycophenolate mofetil
Thymectomy
Plasma exchange
Immunoglobulin infusions

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