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Ventricular tachycardia: a presentation of Fabry disease case report

BACKGROUND: Fabry disease is an inherited rare metabolic disease caused by mutation in the GLA gene, encoding lysosomal enzyme alpha-galactosidase A. The disorder is a systemic disease that manifests as cerebrovascular and cardiac disease, chronic renal failure, skin lesion, peripheral neuropathy, a...

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Detalles Bibliográficos
Publicado en:Eur Heart J Case Rep
Main Authors: Pavlu, Ludek, Kocourkova, Lenka, Taborsky, Milos, Petrkova, Jana
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2018
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6439386/
https://ncbi.nlm.nih.gov/pubmed/31020230
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ehjcr/yty154
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