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 …

HHT have variants of unknown significance or no detectable mutations in any of the above-
listed genes suggesting involvement of alternative pathways and mechanisms. De novo …

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular disorder
that can involve the liver diffusely in the form of vascular malformations ranging from small …

Object Studies on the efficacy of arteriovenous malformation (AVM) radiosurgery have
largely been conducted in the adult population. Clinically, the results may not always be …

BACKGROUND: Patients diagnosed with hereditary hemorrhagic telangiectasia (HHT) are
at risk of developing intracranial arteriovenous malformations (AVM). However, the clinical …

Objective Pediatric pial arteriovenous fistulae (pAVF) are rare vascular lesions of the CNS,
reported to have up to a 25% association with hereditary hemorrhagic telangiectasia. The …

Object Hereditary hemorrhagic telangiectasia (HHT) is a hereditary disorder characterized
by mucocutaneous telangiectasias, frequent nosebleeds, and visceral arteriovenous …

Hereditary haemorrhagic telangiectasia (HHT) is characterized by the development of
arteriovenous malformations—enlarged shunts allowing arterial flow to bypass capillaries …

BACKGROUND Cerebral arteriovenous malformations (AVMs) are common in patients with
hereditary hemorrhagic telangiectasia (HHT). However, due to the rarity of HHT and little …

Objective and importance Complete spontaneous obliteration of a brain arteriovenous
malformation (AVM) is a rare event, with 67 angiographically proven cases in the world …