Concurrent fabry disease and immunoglobulin a nephropathy: a case report

BACKGROUND: Fabry disease (FD) is an X-linked, hereditary dysfunction of glycosphingolipid storage caused by mutations in the GLA gene encoding alpha-galactosidase A enzyme. In rare cases, FD may coexist with immunoglobulin A nephropathy (IgAN). We describe a case of concurrent FD, IgAN, and dilated...

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Detalles Bibliográficos
Autores principales: Zhou, Li-Na, Dong, Shao-Shao, Zhang, Sheng-Ze, Huang, Li-Wa, Huang, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621085/
https://www.ncbi.nlm.nih.gov/pubmed/37914990
http://dx.doi.org/10.1186/s12882-023-03282-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621085/
https://www.ncbi.nlm.nih.gov/pubmed/37914990
http://dx.doi.org/10.1186/s12882-023-03282-3

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