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Lysosomal Storage Disease

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plusmarek's version from 2016-05-10 04:10

Section

Question Answer
Fabry Diseasea-galactosidase A; ceramide trihexoside, XR
Gaucher DiseaseGlucocerebrosidase, Glucocerebroside
Niemann-Pick DiseaseSphingomyelinase; Sphingomyelin
Tay-Sachs DiseaseHexosaminidase A; GM2 ganglioside
Krabbe DiseaseGalactocerebrosidase; Galactocerebroside; psychosine
Metachromatic LeukodystrophyArylsulfatase A; Cerebroside sulfate
Hurler Syndromea-L-iduronidase; Heparine Sulfate and dermatan sulfate
Hunter SyndromeIduronate sulfatase; Heparan sulfate and dermatan sulface (XR)
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