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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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| Vydáno v: | Eur Heart J Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2018
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| Témata: | |
| On-line přístup: | 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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