Results 81 to 90 of about 1,710,432 (174)

Hereditary Hemorrhagic Telangiectasia or Osler-Weber -Rendu Syndrome: Management of Epistaxis in 4 Cases [PDF]

open access: yes, 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
core   +1 more source

ChatGPT Generated Otorhinolaryngology Multiple‐Choice Questions: Quality, Psychometric Properties, and Suitability for Assessments

open access: yesOTO 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 of liver: Pathophysiology with role of radiology in diagnosis and treatment

open access: yesIndian 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

Coexistence of brain capillary telangiectasia and venous angioma: A case report and literature review

open access: yesClinical 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

Síndrome de Osler-Weber-Rendu

open access: yes, 2009
Tres imágenes de un síndrome de Osler-Weber-Rendu.Three pictures of a Osler-Weber-Rendu ...
Iglesias Rozas, José Rafael, 1942-
core  

Severe Hepatic and Pulmonary Involvement in Rendu-Osler-Weber Syndrome

open access: yesCase Reports in Gastroenterology, 2018
We report the case of a young woman with hereditary hemorrhagic telangiectasia (HHT) with severe liver involvement and pulmonary shunting. The medical imaging in this patient illustrates the severe shunting that can occur in these patients who often are ...
Xavier Verhelst   +4 more
doaj   +1 more source

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

open access: yes, 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
core   +1 more source

Case of Osler-Weber-Rendu Syndrome Complicated with Nasal Septum Perforation

open access: yesCentral 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

High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia

open access: yesEuropean Journal of Neurology, Volume 31, Issue 2, February 2024.
Abstract Background and purpose Hereditary haemorrhagic telangiectasia (HHT) is a genetic disease with fragile blood vessels and vascular malformations, potentially causing neurological manifestations, including stroke and cerebral abscesses. The study aimed to investigate neurological manifestations in the Danish HHT database, focusing on pulmonary ...
Mikkel Seremet Kofoed   +5 more
wiley   +1 more source

Endoglin mutants retained in the endoplasmic reticulum exacerbate loss of function in hereditary hemorrhagic telangiectasia type 1 (HHT1) by exerting dominant negative effects on the wild type allele

open access: yesTraffic, Volume 25, Issue 1, January 2024.
The formation of heterodimers between ER‐retained endoglin mutants and WT endoglin impairs WT maturation and trafficking to the plasma membrane. Abstract Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder affecting 1 in 5000–8000 individuals.
Nesrin Gariballa   +2 more
wiley   +1 more source

Home - About - Disclaimer - Privacy