Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant condition with a
prevalence of~ 1 in 5,000 individuals. The pathophysiology of this condition centers on the …

Background Hereditary haemorrhagic telangiectasia (HHT) is a dominantly inherited genetic
vascular disorder that has prevalence of 1: 5000 to 1: 8000, and which is characterised by …

OBJECTIVE: To describe pregnancy outcomes in women with hereditary hemorrhagic
telangiectasia (HHT). METHODS: This was a retrospective descriptive study of women with …

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular dysplasia
characterized by epistaxis, mucocutaneous telangiectasias, and arteriovenous …

Background Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant
condition. It is rarely seen in pregnancy and even more rarely has uterine manifestations …

Objective To retrospectively describe a large series of pregnancies in women with hereditary
haemorrhagic telangiectasia followed in our reference centre, plus neonatal outcomes, to …

Hereditary haemorrhagic telangiectasia (HHT) displays significant variation in severity
between affected individuals in the same family, ranging from relatively trivial epistaxis and …

BACKGROUND: Hereditary hemorrhagic telangiectasia is a rare but life-threatening disease
characterized by telangiectasias and arteriovenous malformations in different organs. When …

Hereditary hemorrhagic telangiectasia (HHT) is characterized by the presence of multiple
arteriovenous malformations (AVMs) that lack intervening capillaries and result in direct …

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disease in
which abnormal communications between arteries and veins, the so-called telangiectases …