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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Ha, Minsu, Kim, Yoon Jae, Kwon, Kwang An, Hahm, Ki Baik, Kim, Mi-Jung, Kim, Dong Kyu, Lee, Young Jae, Oh, S Paul
Format: Artigo
Jezik:Inglês
Izdano: Baishideng Publishing Group Co., Limited 2012
Teme:
Case Report
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki