Results 31 to 40 of about 1,710,432 (174)
Fibrodysplastic implications for transvenous embolization of a high-flow pelvic arteriovenous malformation in Osler-Weber-Rendu syndrome. [PDF]
J Vasc Surg Cases, 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 N, Thomas J, Rahimi S.
europepmc +2 more sources
Медицина неотложных состояний, 2023 Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome, Osler-Weber-Rendu disease, etc) is diagnosed clinically according to the so called Curacao criteria, if at least three of four of them are present: recurrent spontaneous epistaxis ...
V.M. Rudichenko +2 more
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Osler–Weber–Rendu syndrome [PDF]
QJM, 2016 Learning points for clinicians Gastrointestinal bleeding occurs in about one-third of patients with Hereditary Hemorrhagic Telangiectasia, however, it contributes less frequently to iron deficiency anemia in patient than unrecognized nasal bleeding. Early recognition with localized management is important.
M U, Butt, E, Yoo, U, Khan
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Investigation of cardiovascular characteristics in a patient with hereditary hemorrhagic telangiectasia, a case report. [PDF]
Physiol RepAbstract Hereditary Hemorrhagic Telangiectasia (HHT) may present with symptoms arising from multiple organ systems. In this case report, the focus is on cardiovascular manifestations, including total blood volume, cardiac function, and the potential role of the sympathetic nervous system (SNS) in the clinical picture. The commonly held supposition that
Søndergaard S, Madsen S.
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Osler-Weber-Rendu Syndrome [PDF]
Turkiye Klinikleri Journal of Dermatology, 2019 Yetmiş dört yaşındaki erkek olgu, yüzünde ve oral mukozada telenjiyektaziler ve sık burun kanaması şikâyetiyle polikliniğimize başvurdu. Olgunun öz geçmişinde, iki kere mide kanaması geçirdiği ve sık burun kanama öyküsü olduğu anlaşıldı.
An, İsa, İsa AN
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Anais Brasileiros de Dermatologia, 2014 Rendu-Osler-Weber Syndrome also known as Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia, with dominant autosomal inheritance.
Sheila Itamara Ferreira do Couto Meireles +4 more
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Rendú Osler Weber Syndrome; case report
Radiology Case Reports, 2022 Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber disease, is a dominant autosomal disease characterized by the presence of multiple telangiectasia in skin and mucus, associated with arteriovenous malformations (AVM) of various organs ...
Oscar Manuel García Córdova, MD +3 more
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Rendu-Osler-Weber syndrome: dermatological approach [PDF]
Anais Brasileiros de Dermatologia, 2015 The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history.
Aline Blanco Barbosa +5 more
doaj +1 more source
Oman Medical Journal, 2021 A 36-year-old male presented with multiple red spots over the tongue that appeared at the age of 10 years. In the past two decades, he had suffered from recurrent spontaneous episodes of profuse bleeding from the nose and tongue lesions, requiring ...
Abheek Sil +2 more
doaj +1 more source