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26 Cards in this Set

  • Front
  • Back
Type 1 vs Type 2 Meat
Type 1: red meat; slow twitch; stustained action, more mitochondria, oxidative phosphorylation

Type 2: white meat; fast twitch, glycolytic enzymes, fewer mitochondria, GLYCOLYSIS
What is the hallmark feature of muscle atrophy?
Variability in muscle fiber size
What is grouped fiber atrophy?
Loss of mosaicism bc:
motor neuron innvervating muscle fibers die
and surrounding neurons (of opposite type presumably) innervate those fascicles
What is a dystrophy?
Progressive destruction of muscle after birth
What is a congenital myopathy?
Present at work; weakness is fixed and non-progressive
Duchenne MD:
Sex
Age of Onset
Hallmark feature
Affects boys (x-linked)
Onset at age 5-6
FEATURE: Pseudohypertrophy of calves (it's fat, not mm)
Dystrophin gene
Duchenne MD
Becker MD
Elevated CPK
Seen in Duchenne MD at onset; decreases as run out of muscle to destroy
Gower's sign
Duchenne MD--child can't get up on legs without getting on all four limbs and pressing up from thighs
Becker MD:
Age of onset
Clinical course
x-linked (boys)
Due to dystrophin mutation
Onset in 2-16 years
Milder clinical course
Dystrophin activity in Duchenne vs Becker
Duchenne: no dystrophin activity
Becker: some dystrophin activity
Limb-Girdle Muscular Dystrophy:
Presentation
Proximal muscle weakness--trouble combing hair, trouble reaching for things
Mutation in sarcoglycans, caveolin.
i.e., mutations in cytoskeletal proteins; Limb-Girdle Muscular Dysrophy
Distal weakness--in hands, feet.
Myotonic MD
Myotonic Muscular Dystrophy:
Presentation
Myotonia (can't relax muscles)
Hatchet-like face (atrophy of masseters)
Frontal baldness
Selective atrophy of type II fibers.
Steroid use
Selective atrophy of type I fibers.
Myotonic MD
Brain damage in addition to muscle disease.
Mitochondrial myopathies
Dermatomyositis vs Polymyositis:
Cells involved
Fiber damage type
Location of inflammation
Antibody role
Dermatomyositis:
B cells/CD4+
Ischemic Fiber Damage
Inflammation around BVs
Membrane-attack from Ab


Polymyositis:
CD8+ T-cells
Direct fiber damage
inflammation around fibers
Not Ab mediated
Perifascicular atrophy
Dermatomyositis
A skin rash can be seen in this muscle disorder.
Dermatomyositis
Distal and proximal weakness in elderly men.
Inclusion body myositis
Myasthenia gravis:
Pathophys
Ab's x ACh receptor
Increasing weakness with repetitive action.
Myasthenia gravis (can't look up at ceiling for long)
Lambert-Eaton Myasthenic Syndrome:
Patophys
Abs x presynaptic Ca2+ channels
Increasing strength with repetitive action.
Lambert-Eaton myasthenic syndrome