Patients with hereditary haemorrhagic telangiectasia can present with a multitude of
symptoms caused by telangiectasia and arteriovenous malformations in the nose, brain …

Hereditary haemorrhagic telangiectasia is an autosomal dominant genetic disorder of
abnormal vasculature, characterised by telangiectasias and arteriovenous malformations …

Objective: To determine whether patients with hereditary haemorrhagic telangiectasia were
being screened according to international guidelines, and to review recent evidence in order …

Hereditary haemorrhagic telangiectasia is a rare, genetic disorder that can present at any
age. It is characterised by epistaxis, mucocutaneous telangiectasia and visceral …

Abstract Objectives/Hypothesis Hereditary hemorrhagic telangiectasia has long been
viewed as a rare condition. Recent evidence indicates that the disorder is more frequent …

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant condition whose
effects are mediated through deficient blood vessel formation and regeneration, with …

Hereditary haemorrhagic teleangiectasia (HHT) or Rendu-Osler-Weber disease is a genetic
autosomal-dominant disorder characterised by the presence of vascular telangiectases in …

Hereditary hemorrhagic telangiectasia is an inherited disease related to an alteration in
angiogenesis, manifesting as cutaneous telangiectasias and epistaxis. As complications, it …

Hereditary haemorrhagic telangiectasia is a rare systemic autosomal dominantly inherited
disorder of the fibrovascular tissue with a wide variety of clinical manifestations. Diagnosis is …

Hereditary hemorrhagic telangiectasia is an uncommon autosomal dominant disease that
occurs in approximately one in 5,000 to 8,000 persons. This multisystem disorder can affect …