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Gastric angiodysplasia in a hereditary hemorrhagic telangiectasia type 2 patient
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people. Clinical diagnosis of HHT is made when a person presents three of the following four criteria: family history, recurrent nosebleeds, mucocutaneous tel...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Co., Limited
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3332300/ https://ncbi.nlm.nih.gov/pubmed/22553411 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v18.i15.1840 |
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