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Glycogen storage diseases

rename
omranalzobaidi's version from 2015-12-08 18:02

Section

Question Answer
Type 1 ( VGD ) ARGlucose-6-phosphatase ,
Type 2 , ( Pompe ) ARysosomal a, 1-4, glucosidase (acid maltase)
Type 3 (cori's disease) AR1-6 glcosidease debranching enzyme
Type 5 (mcardle's) ARglycogen phosphorylase ( myophosphorylase )
VGDSever fasting hypoglycemia , increase glycogen in the liver , increse blood lactate , hepatomegaly
Pompeearly death
Mcardle Painful muscle cramps , Myoglobinuria ( red urine )
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