| Literature DB >> 22474728 |
Brigitte A Flanagan1, Chris Collins, Sylvia Parra.
Abstract
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal-dominant disorder. The disease has been formally characterized with epistaxis, cutaneous and mucosal telangiectases, a first-degree relative with HHT, and visceral lesions such as arteriovenous malformations (AVMs). Hereditary hemorrhagic telangiectasia has been underreported for many years. Wider recognition of this disorder in recent years has prompted researchers and physicians to recognize milder cases and focus on earlier treatment. This article highlights different treatments used to control epistaxis and screen for other complications associated with HHT.Entities:
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Year: 2012 PMID: 22474728
Source DB: PubMed Journal: Cutis ISSN: 0011-4162