Objective: Hereditary hemorrhagic telangiectasia, or Rendu-Osler-Weber disease, is an
autosomal dominant genetic disorder characterized by abnormal vessel formation …

Background Recurrent epistaxis is the most common manifestation of hereditary
hemorrhagic telangiectasia (HHT). The aim of this study was to determine the role and …

Conclusions: In contrast to the current trend according to which the treatment of hereditary
hemorrhagic telangiectasia (HHT) epistaxis depends on clinical severity, argon plasma …

Patients with hereditary hemorrhagic telangiectasia (M. Osler-Rendu-Weber disease) often
suffer from recurrent epistaxis that poses considerable therapeutic problems. Dermoplasty …

Periodic and spontaneous nosebleed is the most common clinical manifestation of
hereditary haemorrhagic telangiectasia (HHT), present in 95% of patients suffering from this …

Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease is a systemic
autosomal dominant disorder involving blood vessels. Phenotypically, the disease presents …

INTRODUCTION Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-
Rendu syndrome, is an autosomal dominant vascular disease with an incidence of …

Objective: To propose radiofrequency coblation as a potential treatment modality for mild to
moderate epistaxis in patients with hereditary haemorrhagic telangiectasia. Method: Case …

The aim of this study was to assess the value of topically applied estrogens in patients with
hereditary hemorrhagic telangiectasia. Twenty-six patients with this disorder were treated …

Objectives Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant
disease characterised by epistaxis. Surgical procedures for epistaxis vary from …