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

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 mutat...

Source: Orphanet Journal of Rare Diseases - November 22, 2016 Category: Internal Medicine Authors: Anette Kjeldsen, Katrine Saldern Aagaard, Pernille Mathiesen T ørring, Sören Möller and Anders Green Source Type: research