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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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| Publicat a: | Cardiovasc Diagn Ther |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
AME Publishing Company
2021
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| Matèries: | |
| Accés en línia: | 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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