Results 11 to 20 of about 5,408,282 (157)

Ischemic cholangitis: Lethal complication of Osler-Weber-Rendu disease [PDF]

open access: yesRadiology Case Reports
Osler-Weber-Rendu disease (OWRD), also known as hereditary haemorrhagic telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by arteriovenous malformations in several organs.
Ouiam Elmqaddem   +5 more
doaj   +3 more sources

Osler-Weber-Rendu disease: A rare cause of recurrent hemoptysis

open access: yesLung 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

Osler-Weber-Rendu syndrome complicated with pulmonary arteriovenous malformation: A case report and review of literatures

open access: yesJournal 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
doaj   +2 more sources

Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case [PDF]

open access: yesEuropean 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
doaj   +2 more sources

Congestive cirrhosis in Osler-Weber-Rendu syndrome: A rare case report

open access: yesRadiology 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
doaj   +2 more sources

Recurrent Gastrointestinal Bleeding in a Man with Osler-Weber-Rendu Syndrome and Intestinal Varices [PDF]

open access: yesCanadian 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
doaj   +2 more sources

Osler-Weber-Rendu Disease Uncovered by Preeclampsia in a Case Report

open access: yesCase Reports in Obstetrics and Gynecology, 2020
Osler-Weber-Rendu disease (OWRD), called hereditary hemorrhagic telangiectasia, is an uncommon genetic illness with the dominant autosomal transmission.
Jamal Ouachaou   +7 more
doaj   +2 more sources

Enfermedad de Rendu-Osler-Weber Rendu-Osler-Weber syndrome

open access: yesRevista 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   +1 more source

Final observation of an extremely severe case of Osler-Weber-Rendu disease in teaching at the pregraduate and postgraduate stages of education and the use of current English-language Internet applications for doctors and patients

open access: yesМедицина неотложных состояний, 2023
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome, Osler-Weber-Rendu disease, etc) is diagnosed clinically according to the so called Curacao criteria, if at least three of four of them are present: recurrent spontaneous epistaxis ...
V.M. Rudichenko   +2 more
doaj   +1 more source

Left extended hepatectomy with biliary resection and reconstruction for hilar cholangiocarcinoma in patient with Osler-Rendu-Weber disease: a case report and review of literature. [PDF]

open access: yesUpdates Surg
: Osler-Rendu-Weber syndrome is a genetic disease that involves organs, liver included, characterized by alterations in the vessel walls, making them more vulnerable to spontaneous rupture and bleeding indeed.
Marchese A   +7 more
europepmc   +2 more sources

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