Results 11 to 20 of about 5,408,332 (199)
Journal of Medical Sciences, 2015 Osler-Weber-Rendu syndrome is a hereditary disease which is diagnosed by criterions of clinical symptoms and examinations. Here, we report a definite case of Osler-Weber-Rendu syndrome who had epistaxis, skin telangiectasia, and pulmonary arteriovenous ...
Kuan-Yu Wang, Jen-Chih Chen, Jane-Yi Hsu
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Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case [PDF]
European Journal of Case Reports in Internal Medicine, 2020 Rendu-Osler-Weber syndrome is a rare inherited syndrome with autosomal dominant transmission characterized by systemic arteriovenous malformations (AVMs) with multi-organ involvement.
Maria Inês Silva +5 more
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The Rendu-Osler-Weber Disease Revealed by a Refractory Hypoxemia and Severe Cerebral Fat Embolism [PDF]
Case Reports in Critical Care, 2013 The Rendu-Osler-Weber disease is a genetic disease which may lead to severe hemorrhage and less frequently to severe organ dysfunction. We report the case of a 22-year-old patient with no personal medical history who was involved in a motorcycle accident
Leonel Barreto +6 more
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Congestive cirrhosis in Osler-Weber-Rendu syndrome: A rare case report
Radiology Case Reports, 2018 Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome is a rare autosomal dominant vascular disorder characterized by epistaxis, mucocutaneous telangiectasias, and arteriovenous malformations affecting various organs and systems.
Patrícia Leitão, PhD +4 more
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Recurrent Gastrointestinal Bleeding in a Man with Osler-Weber-Rendu Syndrome and Intestinal Varices [PDF]
Canadian Journal of Gastroenterology, 1988 A patient with Osler-Weber-Rendu disease and idiopathic intestinal varices who presented with recurrent gastrointestinal hemorrhage and iron deficiency anemia is reported. The unique coexistence of these two rare disorders is discussed and the literature
Robert N. Clark +3 more
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A Case Report on Osler -Weber Rendu Disease [PDF]
International Journal of Hematology and Blood Disorders, 2019 Osler weber rendu disease, also known as hereditary hemorrhagic telengiectasia is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in skin, mucous membrane and in organs such as lungs, liver and brain. A 68 year old postmenopausal lady was admitted to our hospital following multiple episodes of hematemesis and ...
Ameez S Khan, Samah Muhammed Salih
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A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome
Medicina, 2022 Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia (HHT), is a rare, autosomal dominant condition that affects approximately 1 in 5000 patients causing abnormal blood vessel formation.
Anna Jargielo +3 more
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Bevacizumab for Refractory Gastrointestinal Bleeding in Rendu-Osler-Weber Disease
GE: Portuguese Journal of Gastroenterology, 2017 Rendu-Osler-Weber disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder which is often characterized by recurrent epistaxis, mucocutaneous and gastrointestinal telangiectasias, and visceral arteriovenous ...
Carlos Bernardes +4 more
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Partial hepatectomy for a patient with Rendu–Osler–Weber disease: a case report
Surgical Case Reports, 2023 Background Rendu–Osler–Weber disease (Osler disease) is a genetic disease with an autosomal dominant inheritance pattern. It is characterized by widespread telangiectasia in multiple organs. Liver involvement of FNH is relatively common, but liver cancer
Naoko Sekiguchi +9 more
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Enfermedad de Rendu-Osler-Weber Rendu-Osler-Weber syndrome
Revista Cubana de Medicina, 2009 La telangiectasia hemorrágica hereditaria o enfermedad de Rendu-Osler-Weber es autosómica dominante, se caracteriza por la presencia de múltiples telangiectasias en piel y mucosas asociadas a malformaciones arteriovenosas de distintos órganos.
Gloria Astencio Rodríguez +5 more
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