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Enzyme Replacement Therapy and Fabry Kidney Disease

✍ Scribed by David G. Warnock

Book ID
117321782
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
64 KB
Volume
29
Category
Article
ISSN
0149-2918

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## ABSTRACT Fabry disease is a multisystem disorder associated with wide variability in clinical expression. Fabry disease is an X‐linked lysosomal storage disorder caused by a deficiency of α‐galactosidaseΒ A. The enzyme defect leads to the systemic accumulation of glycosphingolipids with α‐galacto

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