Results 11 to 20 of about 3,185 (193)

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, Jean-Bernard Amiel, Anthony Dugard, Nicolas Pichon, Marc Clavel, Bruno François, Philippe Vignon   +6 more
doaj   +2 more sources

Malformações arteriovenosas pulmonares na síndrome de Rendu-Osler-Weber [PDF]

Jornal Vascular Brasileiro
Resumo A síndrome de Rendu-Osler-Weber, também conhecida como telangiectasia hemorrágica hereditária, é uma doença hereditária autossômica dominante. Ela é caracterizada pela presença de múltiplas malformações arteriovenosas e telangiectasias.
Cristiane Ferreira de Araújo-Gomes, Carlos Eduardo Virgini-Magalhães, Leonardo Silveira de Castro, Eduardo de Oliveira Rodrigues Neto, Alex Antunes Bezerra, Monica Rochedo Mayall, Cristina Ribeiro Riguetti-Pinto, Felipe Borges Fagundes   +7 more
doaj   +3 more sources

Bevacizumab for Refractory Gastrointestinal Bleeding in Rendu-Osler-Weber Disease. [PDF]

GE Port J Gastroenterol, 2018
Bernardes C, Santos S, Loureiro R, Borges V, Ramos G.   +4 more
europepmc   +3 more sources

Lobectomy for Pulmonary Arteriovenous Fistula in a Patient With Rendu-Osler-Weber Disease: A Case Report. [PDF]

In Vivo, 2023
Ishikawa T, Takamori S, Kohno M, Miura N, Takenaka T, Yoshizumi T.   +5 more
europepmc   +3 more sources

Rendu-Osler-Weber syndrome: A family investigation and review

Journal of Indian Academy of Oral Medicine and Radiology, 2009
Rendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency ...
V G Mahima, Karthikeya Patil, Madhur Kapoor, Shalini Kalia   +3 more
doaj   +2 more sources

Hæmorrhagic Telangiectasia of Rendu-Osler-Weber [PDF]

Proceedings of the Royal Society of Medicine, 1946
C. H. Whittle
openaire   +5 more sources

Síndrome Rendu-Osler-Weber como causa de sangrado digestivo alto. Presentación de un caso y revisión de la literatura

Revista Finlay, 2015
Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder of the walls of the blood vessels that become tortuous and dilated. Clinically, patients with this disease develop recurrent bleeding, which may occur spontaneously or following ...
Rodolfo Morales Valdés, Mario Orlando Hernández Cubas, Mailyn Acosta Álvarez, Javier Cruz Rodríguez, Joel Ramos Rodríguez, Yohny Calle Caspa   +5 more
doaj   +3 more sources

Osler-Weber-Rendu Syndrome as a Rare Cause of Liver Cirrhosis. [PDF]

Cureus
Tuna C, Frazão T, Garcês Soares S, Silva MJ, Pinho I, Presa Ramos J.   +5 more
europepmc   +3 more sources

OSLER – WEBER – RENDU SYNDROME: A RARE CASE OF UPPER GASTROINTESTINAL BLEEDING

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, Muhammad Ahmed Khan, Sumera Akram   +2 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

Медицина 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, N.V. Snigir, V.О. Кrivets   +2 more
doaj   +1 more source