Results 31 to 40 of about 3,185 (193)
Clinical Case Reports, 2023 Osler‐Weber‐Rendu syndrome is an uncommon vascular disorder inherited as an autosomal dominant trait with varying penetrance and expression. A multidisciplinary approach is used for a detailed diagnostic workup and management based on the patient's ...
Sulav Pyakurel +7 more
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Osler-Weber-Rendu disease: A rare cause of recurrent hemoptysis
Lung India, 2016 Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant condition causing systemic fibrovascular dysplasia. It has an incidence of 1-2/100,000. Phenotypic variation is extreme ranging from asymptomatic
Amir M Khoja +3 more
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Pulmonary arteriovenous malformation
Journal of the Belgian Society of Radiology, 2011 A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
E Janssens +4 more
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[Rendu-Osler-Weber disease]. [PDF]
Nederlands tijdschrift voor tandheelkunde, 2005 Rendu-Osler-Weber disease or hereditary hemorrhagic telangiectasia (HHT) is a multisystem autosomal dominant hereditary disorder. The disorder is manifested by multiple dysplasia of blood vessels of the skin and mucous membranes. This results in recurrent and sometimes severe bleeding, of which epistaxis is the most common.
Sys, L.M., Hoogen, F.J.A. van den
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Massive Hemothorax by Ruptured Arteriovenous Malformation [PDF]
Modern MedicineIntroduction and objectives: Osler Weber Rendu disease is a rare genetic disorder characterized by multiple telangiectasias and arteriovenous malformations involving parenchymatous organs, leading to hemorrhagic, sometimes life threatening vascular ...
Genoveva CADAR, Otilia RADU
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Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case
European Journal of Case Reports in Internal Medicine, 2020 Rendu-Osler-Weber syndrome is a rare inherited syndrome with autosomal dominant transmission characterized by systemic arteriovenous malformations (AVMs) with multi-organ involvement.
Maria Inês Silva +5 more
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Hereditary Hemorrhagic Telangiectasia
Pediatric Neurology Briefs, 1998 Hereditary Hemorrhagic Telangiectasia (HHT), also known as Osler-Weber-Rendu disease, was the subject of an NIH workshop, organized by the National Heart, Lung, and Blood Institute, on July 10-11, 1997.
J Gordon Millichap
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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
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Case of Osler-Weber-Rendu Syndrome Complicated with Nasal Septum Perforation
Central 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
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A Spinal Arteriovenous Fistula in a 3-Year Old Boy
Case Reports in Pediatrics, 2014 We present a case of a 3-year-old boy with neurodegeneration. Family history reveals Rendu-Osler-Weber disease. Magnetic resonance imaging (MRI) of the spinal cord and spinal angiography showed a spinal ...
Thomas E. M. Crijnen +6 more
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