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 GLA gene mutations. This disorder leads to intracellular globotriaosylceramide (Gb3) deposition associated with increased Gb3 plasma levels. Most of the symptoms of the...

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Detalles Bibliográficos
Autores principales: Capelli, Irene, Aiello, Valeria, Gasperoni, Lorenzo, Comai, Giorgia, Corradetti, Valeria, Ravaioli, Matteo, Biagini, Elena, Graziano, Claudio, La Manna, Gaetano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353860/
https://www.ncbi.nlm.nih.gov/pubmed/32532136
http://dx.doi.org/10.3390/medicina56060284

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353860/
https://www.ncbi.nlm.nih.gov/pubmed/32532136
http://dx.doi.org/10.3390/medicina56060284

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