Results 91 to 100 of about 5,408,332 (199)

Osler-Weber-Rendu syndrome - Pathological manifestations and autopsy considerations

open access: yes, 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.
core   +1 more source

Fibrodysplastic implications for transvenous embolization of a high-flow pelvic arteriovenous malformation in Osler-Weber-Rendu syndrome [PDF]

open access: yes, 2015
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
core   +1 more source

A new ENG mutation in a Japanese family with hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

open access: yesRespiratory Medicine Case Reports, 2018
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

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2006
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

open access: yes
United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley   +1 more source

Enfermedad de Rendú-Osler-Weber: a propósito de 5 casos con epístaxis recurrente Rendú-Osler-Weber disease: apropos of 5 cases with recurrent epistaxis

open access: yesRevista Cubana de Hematología, Inmunología y Hemoterapia, 2012
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  

Effect of Transcriptional Regulator ID3 on Pulmonary Arterial Hypertension and Hereditary Hemorrhagic Telangiectasia

open access: yesInternational Journal of Vascular Medicine, 2019
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]

open access: yes, 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
core  

Hereditary hemorrhagic teleangiectasis (Rendu-Osler-Weber Syndrome) as cause for stomach hemmorrhage - case report [PDF]

open access: yes, 2009
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
core   +1 more source

Doppler ultrasound findings in Osler-Weber-Rendu disease with hepatic involvement: a case report

open access: yes, 1994
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
core  

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