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Article

Renal transplantation between siblings with unrecognized Fabry disease.

Transplantation proceedings - 1 Jan 2000

Taneda S, Honda K, Nakajima I, Huchinoue S, Oda H

Abstract excerpt

Fabry disease is an X-linked lysosomal storage disease caused by deficiency of the lysosomal hydrolase, α-galactosidase A (α-Gal A). We report a case of a renal transplant recipient with unrecognized Fabry disease who received the allograft from a sibling donor with unrecognized Fabry disease. The recipient began to show a gradual increase of the serum creatinine with mild proteinuria at 3 years after...

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Identifiers

PMID: 23375284
DOI: 10.1016/j.transproceed.2012.10.024

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