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Hereditary Hemorrhagic Telangiectasia and Myocardial Infarction
Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu syndrome, is an autosomal dominant genetic disorder that leads to epistaxis, gastrointestinal bleeding, iron deficiency anemia, and arteriovenous malformations at the lungs, the liver, and the brain. However, due to its rarity an...
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| Publicado no: | Int J Angiol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Thieme Medical Publishers
2015
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5186306/ https://ncbi.nlm.nih.gov/pubmed/28031662 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0035-1551795 |
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