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Hereditary Hemorrhagic Telangiectasia in a Sudanese Patient
BACKGROUND: Hereditary hemorrhagic telangiectasia (HHT) also known as Osler–Weber–Rendu syndrome is a rare autosomal dominant disorder, which results in vascular dysplasia affecting mainly visceral and mucocutaneous organs. Case Presentation. A 65-year-old woman with a 12-year history of recurrent s...
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| Gepubliceerd in: | Case Rep Med |
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| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Hindawi
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7752298/ https://ncbi.nlm.nih.gov/pubmed/33414829 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/6395629 |
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