Results 71 to 80 of about 411,420 (197)
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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Multiple Cerebral Angiomas and Rendu-Osler-Weber Disease: Case Report
, 1991 A 25-year-old man was hospitalized after suffering a subarachnoid hemorrhage. Arteriograms disclosed two arteriovenous malformations, one of which was asymptomatic. Rendu-Osler-Weber disease was suspected because of the concomitant existence of cutaneous
M. Jan +3 more
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High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia
European 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
Traffic, 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
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 +7 more
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Neurologic Manifestation as Initial Presentation in a Case of Hereditary Haemorrhagic Telangiectasia
Clinical Medicine Insights: Case Reports, 2010 Hereditary Haemorrhagic Telangiectasia (HHT), or Osler-Weber-Rendu syndrome is an uncommon autosomal dominant multi-organ condition of vascular dysplasias.
Yeow Kwan Teo, Ai Ching Kor
doaj +1 more source
Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience.
, 2011 BACKROUNDS/PURPOSE: Hereditary hemorrhagic telangiectasia or Rendu-Weber-Osler is an autosomal dominant inherited disorder characterized by arteriovenous malformations and telangiectasia that may affect the nose, skin, lungs, brain and gastrointestinal ...
Philippe Wolf +17 more
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Osler-Weber-Rendu syndrome - Pathological manifestations and autopsy considerations
, 2001 An 18-year-old university student with Osler-Weber-Rendu disease collapsed in the bathroom. Attempted resuscitation was unsuccessful. Her past history included recurrent epistaxes, mucosal telangiectasias, intracranial arteriovenous malformations with ...
Byard, R., Schliebs, J., Koszyca, B.
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Rendu-Osler-Weber Syndrome: A Case Report [PDF]
, 2020 Hereditary hemorrhagic telangectasia (HHT) or Rendu-Osler-Weber syndrome, is a rare genetic disorder with autosomal dominance and variable penetrance. The typical findings of the disease are telangiectasias in skin and mucous membranes, and arteriovenous
Vladimir Vukomanović +3 more
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