Fabry disease: what the cardiologist should consider in non-cardiac screening, diagnosis, and management—narrative review

Fabry disease (FD) is a rare X chromosomally transmitted lysosomal storage disorders with an absence or deficiency of the enzyme alpha-galactosidase. The deposition of globotriaosylceramide (Gb3) may cause damage to all organs, particularly brain, heart and kidney. While acroparaesthesia, hypo- or a...

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Bibliografische gegevens
Gepubliceerd in:Cardiovasc Diagn Ther
Hoofdauteurs: Regenbogen, Claudia, Braunisch, Matthias Christoph, Schmaderer, Christoph, Heemann, Uwe
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: AME Publishing Company 2021
Onderwerpen:
Review Article on Current Management Aspects in Adult Congenital Heart Disease (ACHD): Part III
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8102250/
https://ncbi.nlm.nih.gov/pubmed/33968643
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/cdt-20-845
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