Hereditary Haemorrhagic Telangiectasia with Severe Anemia and Recurrent CNS Infections.

Abstract

Hereditary Haemorrhagic Telangiectasia, also known as Osler-Rendu-Weber disease is a rare autosomal dominant disorder affecting small vessels of multiple systems whose main pathological change is the presence of abnormal arteriovenous communications. Usually presents as skin and mucosal telangiectasias, epistaxis, gastrointestinal bleeding and visceral… (More)

5 Figures and Tables

Topics

  • Presentations referencing similar topics