Kidney Transplant in Fabry Disease: A Revision of the Literature
Fabry disease is classified as a rare X-linked disease caused by a complete or partial defect of enzyme alpha-galactosidase, due to <i>GLA</i> gene mutations. This disorder leads to intracellular globotriaosylceramide (Gb3) deposition associated with increased Gb3 plasma levels. Most of the symptoms...
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| Hauptverfasser: | , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
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MDPI AG
2020-06-01
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| Schriftenreihe: | Medicina |
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| Online-Zugang: | https://www.mdpi.com/1648-9144/56/6/284 |
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