Results 101 to 110 of about 1,710,432 (184)

Rendu-Osler-Weber Syndrome With Big Pulmonary Artero-Venous Malformation (Pavm) And Associated Foramen Ovale Patency (Fop)

, 2019
A 55 years old woman with a personal history of brain abscesses, recurrent epistaxis and transient ischemic attacks, underwent Mininvasive Surgery with atrial septal device positioning.
Francesco Inzirillo, Marialuisa Di Matteo, Claudio Della Pona   +2 more
core   +1 more source

Maladie de Rendu-Osler. Manifestations cliniques et prise en charge multidisciplinaire [Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): clinical manifestations and multidisciplinary management]

, 2016
Hereditary hemorrhagic telangiectasia (HHT), or Osler- Weber-Rendu syndrome, is a rare genetic disorder with autosomal dominant inheritance, characterized by recurrent epistaxis, mucocutaneous telangiectasia and visceral arteriovenous malformations (AVMs)
Frigerio, C., Fellmanne, F., Qanadli, S.D., Mazzolai, L., Lazor, R., Baud, D., Ikonomidis, C., Aebischer, N., Bonafe, L., Michel, P., Nichita, C.   +10 more
core   +1 more source

Rendu-Osler-weber disease. Case report [PDF]

, 2016
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Kurochkin Sergei Vyacheslavovich, Gafurov Marat, Kurochkin S., Gafurov M., Zidikhanov Damir Ilshatovich, Chuvashaev I., Chuvashaev Iskander, Zidikhanov D.   +7 more
core  

Hereditary Hemorrhagic Telangiectasia or Rendu-Osler-Weber Syndrome in the Same Family

Collegium antropologicum, 2000
The authors present the case of three patients from the same family in whom hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber syndrome was diagnosed. The disease is rare and occurs with multiple telangiectases of the skin and mucosa, and pulmonary arteriovenous fistulae.
Kukulj, S., Ivanovi-Herceg, Z., Slobodnjak, Z.   +2 more
openaire   +2 more sources

Osler-Weber-Rendu Syndrome: a case report [PDF]

, 2016
El síndrome de Rendu-Osler-Weber (SROW), conocido también como Telangiectasia Hemorrágica Hereditaria (THH), es un desorden vascular infrecuente. Se trata de una alteración vascular displásica multisistémica de carácter autosómico dominante, con diversas
Bustamante, Freyli, Tenreiro Picón, Oscar, Tenreiro, Andrea, Bustamante, Ekaterina   +3 more
core  

Reporte de un caso clínico Sindrome de Rendu – Osler – Weber y Sîndrome Antifosfolipido: (Report of a clinical case Rendu – Osler – Weber Syndrome and Antiphospholipid Syndrome)

Rendu-Osler-Weber syndrome (HHT) is a vascular disorder characterized by the presence of telangiectasias and arteriovenous malformations. It is an autosomal dominant multisystem dysplastic vascular disorder.
Pinto Pineda, Verónica Alejandra, Pinto Pineda, Francisco Rafael, Lalama Gómez, Karolin Paulina   +2 more
core   +1 more source

Malignant neoplasm of cecum in Rendu-Osler-Weber syndrome patient.

Wiadomosci lekarskie (Warsaw, Poland : 1960), 2009
The presented case is the another one which ilustates the coexistence of cecum malignancy and genetics-conditional multisystemic arteriovenous malformations. A 64-year-old male with the mucosal form of Rendu-Osler-Weber syndrome presented a history of two different causes of lower gastrointestinal bleeding occurred clinically and confirmed by ...
Marek, Drózdz, Jacek, Gawrychowski, Krzysztof, Szczechowski   +2 more
openaire   +1 more source

Rendu-Osler-weber disease. Case report

, 2020
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Kurochkin Sergei Vyacheslavovich, Gafurov Marat, Kurochkin S., Gafurov M., Zidikhanov Damir Ilshatovich, Chuvashaev I., Chuvashaev Iskander, Zidikhanov D.   +7 more
core  

Reduction of bilateral dislocation of TMJ and Rendu Osler Weber syndrome: case report and physiopathological model. [PDF]

J Surg Case Rep, 2018
Boccalatte LA, Nassif MG, Figari MF.
europepmc   +1 more source

Brain Abscess in a Patient with Rendu-Osler-Weber Syndrome: Value of Proton Magnetic Resonance Spectroscopy. [PDF]

NMC Case Rep J, 2016
Mejía ARR, Fuertes MY, Moya MJ.
europepmc   +1 more source