Disorders of the Musculoskeletal System (Muscle disorders & PNS) Flashcards

1
Q

0-12 year old boys, autosomal recessive, severe-FATAL, PSEUDOHYPERTROPHY of calf muscles, increased CPK 300 times. “X-Linked” Mother to son, Pelvis & Legs. GOWER sign.

A

Erb-Duchenn’s Muscular Dystrophy

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2
Q

10-70 year old, autosomal recessive, mild, Less severe than Duchenne’s , slower, Pelvis and Legs

A

Becker Muscular Dystrophy

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3
Q

10-20 year old, Autosomal Dominant, Mild, affect face and shoulders.

A

Fascioscapulohumeral Dystrophy

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4
Q

Adults, autosomal dominant, slow progression, affects face, tongue and extremities

A

Myotonic Dystrophy

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5
Q

Acute Polyneuropathy, Polyradiculitis, following surgery or immunization, ASCENDING paralysis. TYPE IV hypersensitivity. “Rubbery Legs”

A

Guillian-Barre aka Acute Demyelinating Polyneuritis aka Landry’s Paralysis

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6
Q

What is the aka for Guillian-Barre?

A

Acute Demyelinating Polyneuritis aka Landry’s Paralysis

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7
Q

Female, myoneural junction, decrease ACH receptors**, especially the cranial nerves, ptosis, diplopia, EYES affected first. TYPE II hypersensitivity

A

Myasthenia Gravis aka Erb- Goldflam’s

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8
Q

What is the aka for Myasthenia Gravis?

A

Erb- Goldflam’s

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9
Q

Common with small cell carcinoma (lung), Increased contractions with repeated stimuli. Autoantibodies inhibit presynaptic calcium channels, OPPOSITE of Myasthenia Gravis

A

Lambert-Eaton

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10
Q

Autosomal dominant, Onset in childhood, CALF MUSCLE atrophy, demyelination, Pain

A

Charcot- Marie- Tooth

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11
Q

Autosomal dominant, hyperextensible skin & joints, large artery FRAGILITY. Defective collagen

A

Ehlers-Danlos Syndrome

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12
Q

30-40 year old, myalgia, early fatigue, painful cramps, weakness of exercising muscles

A

McArdle’s

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