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Recurrent Cerebrovascular Complications under Enzyme Replacement Therapy in a Patient with Fabry Disease on Peritoneal Dialysis

Fabry disease is an X-linked lysosomal storage disorder due to mutations in the alpha-galactosidase A gene, which leads to the accumulation of globotriaosylceramide in various organs. In Fabry disease with end-stage renal disease (ESRD), cerebrovascular events are lethal, even with enzyme replacemen...

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Detalles Bibliográficos
Autores principales: Muto, Reiko, Suzuki, Yasuhiro, Shimizu, Hideaki, Yasuda, Kaoru, Ishimoto, Takuji, Maruyama, Shoichi, Ito, Yasuhiko, Mizuno, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017251/
https://www.ncbi.nlm.nih.gov/pubmed/35831104
http://dx.doi.org/10.2169/internalmedicine.0185-22