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Successful treatment of bleeding gastro-intestinal angiodysplasia in hereditary haemorrhagic telangiectasia with thalidomide

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterised by epistaxis, cutaneous telangiectasia and visceral arterio-venous malformations (AVMs). It affects approximately one in 5000 people. Control of sustained and repeated haemorrhages from telangiectasias in th...

詳細記述

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書誌詳細
主要な著者: Alam, Mohamed Aftab, Sami, Sarmad, Babu, Sathish
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Publishing Group 2011
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3214210/
https://ncbi.nlm.nih.gov/pubmed/22674103
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.08.2011.4585
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