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Fabry disease during the COVID-19 pandemic. Why and how treatment should be continued
Fabry disease is an X-linked disease due to a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral and renal complications. Eve...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier Inc.
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274950/ https://www.ncbi.nlm.nih.gov/pubmed/32561366 http://dx.doi.org/10.1016/j.ymgme.2020.06.002 |