Hereditary Haemorrhagic Telangiectasia
Subspecialty: Neurovascular
Type: Clinical Summary
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is a genetic vascular disorder marked by the development of arteriovenous malformations (AVMs) and telangiectases, which can lead to significant bleeding risks. Understanding the pathophysiology and manifestations of HHT is crucial for timely diagnosis and management, as affected individuals often experience symptoms such as recurrent epistaxis and gastrointestinal bleeding. This review covers the clinical presentation, diagnostic criteria, and comprehensive management strategies for HHT. Overview HHT has an…