Abstract Osler-Weber-Rendu disease (OWRD), also known as hereditary haemorrhagic
telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by …

Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant vascular
dysplasia in which disrupted angiogenesis leads to increased formation of mucocutaneous …

Résumé La maladie de Rendu-Osler (MRO) est une maladie vasculaire du capillaire,
héréditaire autosomique dominante, rare, avec une prévalence de 1/5000. Elle est …

Rendu-Osler-Weber disease also known as hereditary hemorrhagic telangiectasia (HHT) is
a rare autosomal dominant disorder [1]. It is caused by mutations in the ENG, ACVRL1 or …

Background Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant
inherited vascular disorder that can involve multiple organs, thus can be associated with so …

During pregnancies with hereditary hemorrhagic telangiectasia (HHT), rare severe
complications could be fatal. This study presents a Chinese immigrant with twin gestation …

Aberrations in blood vessel diameters can disrupt hierarchical vascular patterning and
cause severe congenital vascular anomalies, like arteriovenous malformations (AVMs) and …

Abstract [eng] Headache is a common condition among children, adolescents and young
adults that can have negative consequences for quality of life, social activity and even …

Abstract [eng] Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder
associated with alterations of angiogenesis. Heterozygous mutations in the ENG or ACVRL1 …

A malformação arteriovenosa pulmonar é uma condição anômala em que há a
comunicação entre artéria e veia pulmonares ocasionando a formação de shunts da direita …