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Cardiac manifestations in patients with classical or cardiac subtype of Fabry disease
BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder engendered by a deficiency of the enzyme α-galactosidase A, leading to systemic accumulation of glycolipids. Studies have reported that the cardiac subtype of FD has a later onset and minimal extracardiac involvement. However,...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Lippincott Williams & Wilkins
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478196/ https://www.ncbi.nlm.nih.gov/pubmed/32649415 http://dx.doi.org/10.1097/JCMA.0000000000000379 |