Comorbidity among HHT patients and their controls in a 20 years follow-up period
Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant genetic disorder with a wide variety of clinical manifestations due to the presence of multiple arteriovenous malformations in various tiss...
Source: Orphanet Journal of Rare Diseases - Category: Internal Medicine Authors: Katrine Saldern Aagaard, Anette Dr øhse Kjeldsen, Pernille Mathiesen Tørring and Anders Green Tags: Research Source Type: research