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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Autores principales: Ha, Minsu, Kim, Yoon Jae, Kwon, Kwang An, Hahm, Ki Baik, Kim, Mi-Jung, Kim, Dong Kyu, Lee, Young Jae, Oh, S Paul
Formato: Artigo
Lenguaje:Inglês
Publicado: Baishideng Publishing Group Co., Limited 2012
Materias:
Case Report
Acceso en línea: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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