Appropriate management of hereditary hemorrhagic telangiectasia (HHT) is of particular
importance in females, as HHT-mediated modifications of the vascular bed and circulation …

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 …

Objectives/Hypothesis To identify factors influencing the severity of epistaxis in hereditary
hemorrhagic telangiectasia (HHT). Study Design Participants with and without HHT were …

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 …

Objectives The aim of this study (PROSPERO ID: CRD42017081952) was to evaluate
medical treatment for epistaxis from hereditary hemorrhagic telangiectasia (HHT). Data …

Background: Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disorder known
for its debilitating symptoms. More than 90% of patients with HHT experience epistaxis, and …

Hereditary hemorrhagic telangiectasia (HHT), also known as Osler–Rendu–Weber
syndrome, is a rare autosomal dominant disorder characterized by vascular malformations …

Background Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant
hereditary disorder resulting in vascular dysplasia and formation of arteriovenous …

Objectives/Hypothesis To identify whether relationships exist between epistaxis and
migraines in hereditary hemorrhagic telangiectasia (HHT), to potentially provide further …

Objectives/Hypothesis Hereditary hemorrhagic telangiectasia (HHT) is an autosomal
dominant vascular dysplasia whose hallmark symptom is spontaneous recurrent epistaxis …