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Article

20-year follow-up study of Danish HHT patients—survival and causes of death

22 Nov 2016

Abstract excerpt

BACKGROUND: Hereditary Haemorrhagic Telangiectasia (HHT) is a dominantly inheritable disorder, with a wide variety of clinical manifestations due to presence of multiple arteriovenous manifestations. The most common mutations are found in HHT1 (ENG) and HHT2 (ACVRL1) patients, causing alterations in the TGF-β pathway which is responsible for angiogenesis. Modulations of angiogenesis may influence cancer rates....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 27876060
DOI: 10.1186/s13023-016-0533-9

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