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The Rendu-Osler-Weber syndrome or Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia which bears, as basic defect, an alteration in the elastic and muscle layers of vessel walls, making them more vulnerable to spontaneous ruptures and injuries 1, 2. The disease is autosomal dominant, although in about 20% of the ...
- Rendu-Osler-Weber disease: a gastroenterologist’s perspective
Hereditary hemorrhagic teleangectasia (HHT, or...
- Rendu-Osler-Weber disease: a gastroenterologist’s perspective
12 gru 2022 · Hereditary hemorrhagic telangiectasia (HHT), formerly Osler-Weber-Rendu, is an inherited (autosomal dominant) disease that results in malformed blood vessels (see Image. Telangiectasia on the Tongue).
27 lut 2024 · Hereditary hemorrhagic telangiectasia (HHT; also called Osler-Weber-Rendu syndrome) is an autosomal dominant vascular disorder associated with a variety of clinical manifestations including mucocutaneous telangiectasia, epistaxis, gastrointestinal bleeding, and iron deficiency anemia.
1 maj 2008 · The present investigation reports the case of one patient with Rendu-Osler-Weber syndrome; seen at the ENT Ward at Faculdade de Medicina de Marília and we review the literature and discuss available treatment options.
4 maj 2011 · Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) is a disorder of development of the vasculature characterized by telangiectases and arteriovenous malformations in specific...
7 cze 2019 · Hereditary hemorrhagic teleangectasia (HHT, or Rendu-Osler-Weber disease) is a rare inherited syndrome, characterized by arterio-venous malformations (AVMs or Telangiectasia). The most important and common manifestation is nose bleeds (epistaxis).
We discuss a case of Osler-Weber-Rendu disease causing diffuse cutaneous telangiectasia and hemoptysis. The patient presented with complaints of hemoptysis and was extensively examined and investigated before being diagnosed with Osler-Weber-Rendu disease.
