Treatment of Fabry Nephropathy: A Literature Review

Fabry disease is an X-linked inherited lysosomal storage disorder with a deficiency of α-galactosidase A activity, which results in the intracellular accumulation of globotriaosylceramide (Gb3) and related glycosphingolipids in various organs. Fabry nephropathy is one of the major complications of F...

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Detalles Bibliográficos
Autores principales: Shimohata, Homare, Yamashita, Marina, Yamada, Kota, Hirayama, Kouichi, Kobayashi, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456687/
https://www.ncbi.nlm.nih.gov/pubmed/37629768
http://dx.doi.org/10.3390/medicina59081478

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456687/
https://www.ncbi.nlm.nih.gov/pubmed/37629768
http://dx.doi.org/10.3390/medicina59081478

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