Disorders of the Musculoskeletal System (Muscle disorders & PNS) Flashcards
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.
Erb-Duchenn’s Muscular Dystrophy
10-70 year old, autosomal recessive, mild, Less severe than Duchenne’s , slower, Pelvis and Legs
Becker Muscular Dystrophy
10-20 year old, Autosomal Dominant, Mild, affect face and shoulders.
Fascioscapulohumeral Dystrophy
Adults, autosomal dominant, slow progression, affects face, tongue and extremities
Myotonic Dystrophy
Acute Polyneuropathy, Polyradiculitis, following surgery or immunization, ASCENDING paralysis. TYPE IV hypersensitivity. “Rubbery Legs”
Guillian-Barre aka Acute Demyelinating Polyneuritis aka Landry’s Paralysis
What is the aka for Guillian-Barre?
Acute Demyelinating Polyneuritis aka Landry’s Paralysis
Female, myoneural junction, decrease ACH receptors**, especially the cranial nerves, ptosis, diplopia, EYES affected first. TYPE II hypersensitivity
Myasthenia Gravis aka Erb- Goldflam’s
What is the aka for Myasthenia Gravis?
Erb- Goldflam’s
Common with small cell carcinoma (lung), Increased contractions with repeated stimuli. Autoantibodies inhibit presynaptic calcium channels, OPPOSITE of Myasthenia Gravis
Lambert-Eaton
Autosomal dominant, Onset in childhood, CALF MUSCLE atrophy, demyelination, Pain
Charcot- Marie- Tooth
Autosomal dominant, hyperextensible skin & joints, large artery FRAGILITY. Defective collagen
Ehlers-Danlos Syndrome
30-40 year old, myalgia, early fatigue, painful cramps, weakness of exercising muscles
McArdle’s