Results 91 to 100 of about 5,408,332 (199)
Osler-Weber-Rendu syndrome - Pathological manifestations and autopsy considerations
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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Fibrodysplastic implications for transvenous embolization of a high-flow pelvic arteriovenous malformation in Osler-Weber-Rendu syndrome [PDF]
Osler-Weber-Rendu syndrome is a rare genetic disorder that commonly features high-flow arteriovenous malformations (AVM) within the pulmonary, intracranial, and visceral circulation.
Nassiri, Naiem +2 more
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We present a case series of four siblings with hereditary hemorrhagic telangiectasia (HHT) and pulmonary arteriovenous malformations (PAVM). The patients' mother has HHT. Case 1: A 22-year-old man developed dyspnea and epistaxis. CT revealed a large PAVM,
Keiki Yokoo +11 more
doaj +1 more source
Angiomatosis in Klippel-Trenaunay -Weber Syndrome - Report of a rare Case
Hemangioma is an abnormal proliferation of blood vessels that may occur in any vascularized tissue. Considerable debate exists as to whether these lesions are neoplasms, hamartomas, or vascular malformations.
G S Kodhandarama +2 more
doaj
UEG Week 2025 Poster Presentations
United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley +1 more source
Los pacientes con epístaxis representan entre el 10 y 12 % de los casos atendidos en los servicios de urgencia de otorrinolaringología. Se presentan 5 pacientes atendidos en este servicio del Hospital General Docente "Enrique Cabrera", en el período ...
Tahamara Alcalá-Villalón +2 more
doaj
Pulmonary arterial hypertension (PAH) can be discovered in patients who have a loss of function mutation of activin A receptor-like type 1 (ACVRL1) gene, a bone morphogenetic protein (BMP) type 1 receptor.
Vincent Avecilla
doaj +1 more source
Rendu-Osler-Weber Syndrome: A Case Report [PDF]
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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Hereditary hemorrhagic teleangiectasis (Rendu-Osler-Weber Syndrome) as cause for stomach hemmorrhage - case report [PDF]
U radu je prikazan sedamdesetcetverogodišnji bolesnik s krvarenjem iz probavnog trakta i posljedicnom sideropenicnom anemijom vjetovanom Rendu-Osler-Weber-ovom bolešcu.
Zvonimir Glumpak +5 more
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Doppler ultrasound findings in Osler-Weber-Rendu disease with hepatic involvement: a case report
A case of Osler-Weber-Rendu disease or hereditary haemorrhagic telangiectasia with hepatic involvement diagnosed by Doppler ultrasound is described showing an increased blood flow within the dilated common hepatic artery and multiple aneurysms of the ...
Rapaccini, Gian Ludovico +1 more
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