Rendu-Osler-Weber syndrome

Rendu-Osler-Weber Syndrome, also known as hereditary hemorrhagic telangiectasia, Babington disease, or Goldstein syndrome, is a hereditary disease caused by abnormal development of the vascular wall. Its typical pathological changes are bright red or purplish-red telangiectasias or small vessel dilations in the skin and mucous membranes, leading to mucocutaneous bleeding. It frequently occurs in the gastrointestinal mucosa, causing gastrointestinal bleeding.