Reading...
Play button
Play button
Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
23 Cards in this Set
- Front
- Back
|
Muscle Disorders Associated with Myalgies
|
Mitochondrial myopathies
Inflammatory myopathy Infectious myositis Drug induced myopathies hypothyroid myopathy myoadenylate deaminase deficiency tubular aggregate myopathy x linked myalgia and cramps eosinophilia myalgia syndrome |
|
|
Myopathies associated with contractures
|
mcardle's
tarui's phophoglycerate kinase deficiency phophoglycerate mutase deficiency ldh deficiency debrancher enzyme deficiency paramyotonia hypothyroidism brody's disease rippling muscle disease |
|
|
what are myopathies associated with muscle stiffness?
|
myotonic dystrophy
myotonia congenita paramyotonia congnita proximal myotonic myopathy hyperkalemic periodic paralysis hypothyroid |
|
|
causes of myoglobinuria?
|
prolonged exercise
viral bacterial infxn drugs/toxins nms heat stroke crush injury or trauma severe metabolic abnl inflammatory myopathies limb girdle 2C-2F mcardle's CPT deficiency malignant hyperthermia (central core) |
|
|
myopathy present at birth
|
congenital myotonic dystrophy
centronuclear (myotubular) myopathy congenital fiber type disproportion central core disease nemaline rod myopathy congenital muscular dystrophy lipid storage disease glycogen storage disease |
|
|
myopathy in childhood
|
duchenne
becker emery driefuss fsh limb-girdle dm/pm nemaline centrnuclear central core cpt deficiency pompe's mitochondrial hypokalemia hypocalcemia/hypercalcemia |
|
|
muscular dystrophy in adulthood
|
limb girdle
emery dreifuss fsh becker pm/dm ibm viral pompe's lipid storage debrancher deficiency mitochondrial thyroid/parathyroid adrenal drugs md nemaline centonuclear |
|
|
X linked
|
duchenne
becker emery dreifuss centronuclear/myotubular |
|
|
autosomal dominant
|
fsh, limb girdle, opmd, md, periodic paralysis, paramyotonia congenita, thomsen disease, central core myopathy
|
|
|
autosomal recessive
|
limb-girdle md
metabolic myopathies becker myotonia |
|
|
myopathy and cardiac disease
|
CPEO
Andersen's syndrome pm myotnic dystrophy limb girdle Emery dreifus duchenne becker nemaline pompe's cpt deficiency |
|
|
Distal weakness Myopathy
|
Welander
Warkesberry Nonaka Miyoshi Desmin myopathy myotonic dystrophy fsh scapuloperoneal emerydreifuss pompe's nemaline central core centronuclear inflammatory, ibm debrancher enzyme deficiency oculopharyngodistal myopathy |
|
|
Myopathy ptosis without opthalmoplegia
|
nemaline
central core centronuclear myotonic dystrophy desmin myofibrillar |
|
|
ptosis with opthalmoplegia
|
lems, botulism, mg, opmd, oculopharyngela dystrophy, cpeo
|
|
|
myopathy with prominent neck extensor weakness
|
myotonic dystrophy, isolated neck extensor weakness myopathy, pm, dm, ibm, carnitine def, fsh, hyperparthyroidism
|
|
|
what is the gomori trichrome stain used for?
|
histology and mitochondrial disease
|
|
|
nadh, succinate dehydrogenase stains?
|
mitochondrial
|
|
|
periodic acid schiff stain
|
glycogen storage disease
|
|
|
oil red o
|
lipid storage diseases
|
|
|
congo red, crystal violet
|
amyloid
|
|
|
dysferlin immunostain
|
limb girdle type 2 b
|
|
|
membrane attack complex immunostain
|
dermatomyositis
|
|
|
dystrophin immunostain
|
duchenne/beckers
|
