Results 71 to 80 of about 1,710,432 (184)
Hereditary Hemorrhagic Telangiectasia or Osler-Weber -Rendu Syndrome: Management of Epistaxis in 4 Cases [PDF]
, 2020 Hereditary Hemorrhagic Telangiectasia, also known as Osler-Weber-Rendu Syndrome is an autosomal dominant disorder causing systemic abnormalities of the vascular structure.
BS, Gendeh, H, Salina, PS, Lim
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OTO Open, Volume 8, Issue 3, July–September 2024.Abstract Objective To explore Chat Generative Pretrained Transformer's (ChatGPT's) capability to create multiple‐choice questions about otorhinolaryngology (ORL). Study Design Experimental question generation and exam simulation. Setting Tertiary academic center.
Cecilia Lotto +6 more
wiley +1 more source
Hereditary hemorrhagic telangiectasia: An informative review
Iraqi Journal of Hematology, 2020 Inherited hemorrhagic telangiectasia (HHT or Osler–Weber–Rendu syndrome) is a hereditary condition characterized by malformations of multiple blood vessels (vascular dysplasia), which may lead to bleeding (hemorrhaging).
Neha Rajpurohit +3 more
doaj +1 more source
Rendu Osler Weber Syndrome, a case report and review
Revista Chilena de Dermatología, 2018 La telangiectasia hemorrágica hereditaria (THH) o síndrome Rendu Osler Weber es un trastorno autosómico dominante que lleva a la formación anormal de vasos sanguíneos y se manifiesta como telangiectasias y malformaciones arteriovenosas en piel y órganos internos.
Danae Álvarez +2 more
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Indian Journal of Radiology and Imaging, 2020 Hereditary hemorrhagic telangiectasia (HHT) or Osler–Weber–Rendu syndrome is a rare condition which can result in significant systemic and hepatobiliary abnormalities. Liver involvement in HHT consists primarily of the consequence of various intrahepatic
Maheswaran Viyannan +2 more
doaj +1 more source
Clinical Case Reports, Volume 12, Issue 5, May 2024.Key Clinical Message While Cerebral vascular malformations exhibit distinct clinical and radiographical features, rare instances of coexisting lesions occur. This case report sheds light on the rare coexistence of brain capillary telangiectasia and venous angioma in a patient presenting with a seizure attributed to frontal lobe bleeding.
Moaz O. Moursi +4 more
wiley +1 more source
, 2009 Tres imágenes de un síndrome de Osler-Weber-Rendu.Three pictures of a Osler-Weber-Rendu ...
Iglesias Rozas, José Rafael, 1942-
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Recurrent Gastrointestinal Bleeding in a Man with Osler-Weber-Rendu Syndrome and Intestinal Varices [PDF]
, 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
Laurington R. DaCosta +3 more
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Case of Osler-Weber-Rendu Syndrome Complicated with Nasal Septum Perforation
Central Asian Journal of Medical Sciences, 2020 Objectives: Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is a rare autosomal dominant disorder characterized by multiple mucocutaneous telangiectasias and visceral arteriovenous malformations.
Odgerel Tsogbadrakh +4 more
doaj +1 more source
[A case of Rendu-Osler-Weber syndrome and pulmonary arteriovenous fistula].
Nihon Kyobu Shikkan Gakkai zasshi, 1995 A 65-year-old man with Rendu-Osler-Weber syndrome was admitted to the department of brain surgery at our hospital because of left hemiplegia and a right cerebral mass seen on a computerized tomogram of the brain. A brain abscess was found during surgery. Then the patient had pneumonia.
Nomura, Masaharu +3 more
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