Hereditary haemorrhagic telangiectasia, inherited as an autosomal dominant trait, affects
approximately 1 in 5000 people. The abnormal vascular structures in HHT result from …

Pulmonary arteriovenous malformations (PAVMs) are abnormal direct vascular
communications between pulmonary arteries and veins which create high-flow right-to-left …

Pulmonary arteriovenous malformations (PAVMs) are abnormal vascular structures that
most often connect a pulmonary artery to a pulmonary vein, bypassing the normal …

Hereditary hemorrhagic telangiectasia (HHT), also known by the eponym Osler–Weber–
Rendu syndrome, is a group of related disorders inherited in an autosomal dominant fashion …

OBJECTIVE. Pulmonary arteriovenous malformations (PAVMs) are most often associated
with hereditary hemorrhagic telangiectasia. Untreated, they represent a serious threat due to …

Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease is a genetic
disorder with autosomal dominance and variable penetrance, characterized by epistaxis …

Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder characterized by
epistaxis, telangiectasia, and visceral vascular manifestations. Infectious and ischemic …

Background Pulmonary arteriovenous malformations are abnormal direct connections
between the pulmonary artery and pulmonary vein which result in a right‐to‐left shunt. They …

Pulmonary arteriovenous malformation, a condition most commonly associated with
hereditary hemorrhagic telangiectasia, is an abnormal communication between the …

In this review, we discuss the role of transforming growth factor-beta (TGF-β) in the
development of pulmonary vascular disease (PVD), both pulmonary arteriovenous …