Agalsidase Alfa and Kidney Dysfunction in Fabry Disease

In male patients with Fabry disease, an X-linked disorder of glycosphingolipid metabolism caused by deficient activity of the lysosomal enzyme α-galactosidase A, kidney dysfunction becomes apparent by the third decade of life and invariably progresses to ESRD without treatment. Here, we summarize th...

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Main Authors: West, Michael, Nicholls, Kathy, Mehta, Atul, Clarke, Joe T.R., Steiner, Robert, Beck, Michael, Barshop, Bruce A., Rhead, William, Mensah, Robert, Ries, Markus, Schiffmann, Raphael
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Society of Nephrology 2009
Ábhair:
Clinical Research
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2678048/
https://ncbi.nlm.nih.gov/pubmed/19357250
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2008080870
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