Author/Authors :
Shamsadini, S. kerman university of medical sciences - Department of Dermatology, ايران , Abbasi, M.H. kerman university of medical sciences - Department of Internal Medicine, ايران , Varesvazirian, M. kerman university of medical sciences - Department of Paediatrics, ايران , Shamsadini, A. Afzalipoor Hospital, ايران
Abstract :
Osler-Weber-Rendu disease, also referred to as hereditary haemorrhagic telangiectasia, is a genetic disease, an autosomal dominant disorder characterized by telangiectasias and aneurysms with primary involvement of the mucosa. The reported prevalence of this disease is 1-2 cases per 100 000 population [1].
