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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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| Autors principals: | , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society of Nephrology
2009
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| Matèries: | |
| Accés en línia: | 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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