Results 1 to 10 of about 3,185 (193)

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, Günter Hans Filho, Carolina Faria dos Santos Vicari, Marcelo Zanolli Medeiros, Daíne Vargas Couto, Luiz Carlos Takita   +5 more
doaj   +6 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, Maria Elena Riccioni, Eleonora Gaetani, Veronica Ojetti, Grainne Holleran, Antonio Gasbarrini   +5 more
doaj   +5 more sources

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,
Irini Nikolaou, MD, Vasileios Rafailidis, MD, MSc, PhD, EDiR, Anastasios Kartas, MD, MSc, Konstantinos Kouskouras, MD, PhD, George Giannakoulas, MD, PhD   +4 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, Tania Cristina Pérez Morales, MD, Verónica Andrea del Pilar Barón Hernández, MD, José Sebastián Sotelo Cuéllar, MD   +3 more
doaj   +2 more sources

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, André Carvalho, MD, Conceição Guerra, MD, José Gonçalves, MD, Isabel Ramos, PhD   +4 more
doaj   +2 more sources

Thalidomide as an effective treatment in a case of Osler Weber Rendu syndrome: a case report

Asian Journal of Medical Sciences, 2016
Osler Weber Rendu Syndrome (OWRS), or Hereditary Hemorrhagic telangiectasia (HHT) is an autosomal dominant disease presents with epistaxis, telangiactesia and multiorgan vascular dysplasia.
Titli Bandyopadhyay
doaj   +3 more sources

Rendu-Osler-Weber Disease [PDF]

Circulation, 2001
A 75-year-old man was admitted to the hospital because of transient unconsciousness and dysarthria. Brain CT and MRI demonstrated a recent cerebellar infarction. Physical examination revealed a continuous extracardiac murmur maximally auscultated (Levine III) between the inner edge of the right scapula and the upper thoracic vertebrae.
H, Kataoka, O, Matsuno
openaire   +3 more sources

Partial hepatectomy for a patient with Rendu-Osler-Weber disease: a case report. [PDF]

Surg Case Rep, 2023
Sekiguchi N, Yamada D, Kobayashi S, Sasaki K, Iwagami Y, Tomimaru Y, Noda T, Takahashi H, Doki Y, Eguchi H.   +9 more
europepmc   +3 more sources

Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome. [PDF]

J Vasc Bras
Abstract Rendu-Osler-Weber syndrome, also known as hereditary hemorrhagic telangiectasia, is an autosomal dominant hereditary disorder. It is characterized by presence of multiple arteriovenous malformations (AVMs) and telangiectasias. This article reports two cases of patients with Rendu-Osler-Weber syndrome who had pulmonary AVMs and underwent ...
de Araújo-Gomes CF, Virgini-Magalhães CE, de Castro LS, Rodrigues EO, Bezerra AA, Mayall MR, Riguetti-Pinto CR, Fagundes FB.   +7 more
europepmc   +3 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, Onix César Garib Alpízar, José Napoleón Ventura Blanco, Boris L. Torres Cueva, Nancy de León Rubio, Jorge Luis Hernández   +5 more
doaj   +1 more source