The gastrointestinal (GI) and cutaneous organ systems are closely linked. In part I of this
continuing medical education article, the intricacies of this relationship were explored as …

Background HHT is an autosomal dominant disease with an estimated prevalence of at least
1/5000 which can frequently be complicated by the presence of clinically significant …

Abstract Objectives/Hypothesis Objectives were to assess available information on
hormonal therapy for bleeding in hereditary hemorrhagic telangiectasia (HHT), to determine …

Objective To evaluate the accuracy of the clinical Curaçao criteria in the diagnosis of
hereditary hemorrhagic telangiectasia (HHT) in children and adolescents. Study design This …

Background A variety of modalities are available for the control of recurrent epistaxis in
hereditary hemorrhagic telangiectasia (HHT). Laser ablation, in particular potassium-titanyl …

Abstract Objectives/Hypothesis: Hereditary hemorrhagic telangiectasia (HHT) is associated
with recurrent epistaxis in 90% of cases. Good response to hormone treatment has been …

Background and Objectives Hereditary hemorrhagic telangiectasia (HHT), also known as
Osler–Weber–Rendu disease, causes recurrent mucous membrane hemorrhage, especially …

Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder of blood vessel formation
resulting in mucocutaneous telangiectasias and visceral arteriovenous malformations …

Pulmonary arteriovenous malformations (PAVMs) often occur in children with hereditary
hemorrhagic telangiectasia (HHT). A 14-year longitudinal study of PAVMs in children with …

Systematic screening in hereditary hemorrhagic telangiectasi... : Current Opinion in Pulmonary
Medicine Systematic screening in hereditary hemorrhagic telangiectasia: a review : Current …