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Cardiac MRI in Fabry disease

Fabry disease is a rare, progressive X-linked inherited disorder of glycosphingolipid metabolism due to a deficiency of α-galactosidase A enzyme. It leads to the accumulation of globotriaosylceramide within lysosomes of multiple organs, predominantly the vascular, renal, cardiac, and nervous systems...

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Detalles Bibliográficos
Autores principales:	Umer, Muhammad, Kalra, Dinesh K.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Cardiovascular Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931723/ https://www.ncbi.nlm.nih.gov/pubmed/36818911 http://dx.doi.org/10.3389/fcvm.2022.1075639

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