Results 11 to 20 of about 583,024 (194)
A case of pulmonary arteriovenous malformation in the setting of Rendu Osler Weber syndrome [PDF]
Radiology Case Reports, 2021 Rendu Osler Weber syndrome is a rare disorder, in which arteriovenous malformations are a hallmark feature. We describe the case of a 77-year-old female patient who presented with dyspnea, recurrent epistaxis, and signs of right ventricular heart failure,
George Giannakoulas +2 more
exaly +4 more sources
Rendu-Osler-Weber disease: a gastroenterologist’s perspective [PDF]
Orphanet Journal of Rare Diseases, 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).
Annalisa Tortora +5 more
doaj +5 more sources
Rendu-Osler-Weber syndrome: dermatological approach [PDF]
Anais Brasileiros de Dermatologia, 2015 The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history.
Aline Blanco Barbosa +5 more
doaj +4 more sources
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
doaj +2 more sources
Clinical Case Reports (discontinued), 2023 Osler‐Weber‐Rendu syndrome is an uncommon vascular disorder inherited as an autosomal dominant trait with varying penetrance and expression. A multidisciplinary approach is used for a detailed diagnostic workup and management based on the patient's ...
Sujan Bohara
exaly +3 more sources
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
doaj +3 more sources
OSLER – WEBER – RENDU SYNDROME: A RARE CASE OF UPPER GASTROINTESTINAL BLEEDING [PDF]
Khyber Medical University Journal, 2022 BACKGROUND: Osler-Weber-Rendu syndrome (Hereditary hemorrhagic telengiectasia) cases present with recurrent epistaxis, gastrointestinal bleeding (hematemesis, melena), and arteriovenous malformations involving almost all organs of body.
Farrukh Sher +2 more
doaj +2 more sources
Rendú Osler Weber Syndrome; case report [PDF]
Radiology Case Reports, 2022 Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber disease, is a dominant autosomal disease characterized by the presence of multiple telangiectasia in skin and mucus, associated with arteriovenous malformations (AVM) of various organs ...
Oscar Manuel García Córdova, MD +3 more
doaj +2 more sources
Pulmonary arteriovenous malformation revealing Osler‐Weber‐Rendu disease: A case report
Clinical Case Reports (discontinued), 2022 Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The present case was a 34‐year‐
Herveat Ramanandafy
exaly +2 more sources
Osler-Weber-Rendu disease: A rare cause of recurrent hemoptysis
Lung India, 2016 Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant condition causing systemic fibrovascular dysplasia. It has an incidence of 1-2/100,000. Phenotypic variation is extreme ranging from asymptomatic
Amir M Khoja +3 more
doaj +2 more sources