Atherosclerosis in Fabry Disease—A Contemporary Review

Fabry disease (FD) is a lysosomal storage disorder characterised by a deficiency in the enzyme α-galactosidase A resulting in sphingolipid deposition which causes progressive cardiac, renal, and cerebral manifestations. The case illustrates a patient with FD who died suddenly, and medical examinatio...

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Detalles Bibliográficos
Autores principales: Roy, Ashwin, Umar, Hamza, Ochoa-Ferraro, Antonio, Warfield, Adrian, Lewis, Nigel, Geberhiwot, Tarekegn, Steeds, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509593/
https://www.ncbi.nlm.nih.gov/pubmed/34640440
http://dx.doi.org/10.3390/jcm10194422

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509593/
https://www.ncbi.nlm.nih.gov/pubmed/34640440
http://dx.doi.org/10.3390/jcm10194422

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