Results 11 to 20 of about 411,420 (197)
OSLER – WEBER – RENDU SYNDROME: A RARE CASE OF UPPER GASTROINTESTINAL BLEEDING
Khyber Medical University Journal, 2022 BACKGROUND: Osler-Weber-Rendu syndrome (Hereditary hemorrhagic telengiectasia) cases present with recurrent epistaxis, gastrointestinal bleeding (hematemesis, melena), and arteriovenous malformations involving almost all organs of body.
Farrukh Sher +2 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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Journal of Medical Sciences, 2015 Osler-Weber-Rendu syndrome is a hereditary disease which is diagnosed by criterions of clinical symptoms and examinations. Here, we report a definite case of Osler-Weber-Rendu syndrome who had epistaxis, skin telangiectasia, and pulmonary arteriovenous ...
Kuan-Yu Wang, Jen-Chih Chen, Jane-Yi Hsu
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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
openaire +4 more sources
Anesthetic management of a patient with Osler-Weber-Rendu syndrome with multiple pulmonary arteriovenous malformations and pheochromocytoma for femoral artificial bone replacement: a case report [PDF]
JA Clinical Reports, 2023 Background Osler-Weber-Rendu syndrome is characterized by mucocutaneous telangiectasia and arteriovenous malformations in organs. Anesthesia for patients with Osler-Weber-Rendu syndrome is challenging due to complications and physiological changes.
Toshiharu Hiyoshi +4 more
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Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case [PDF]
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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Recurrent Gastrointestinal Bleeding in a Man with Osler-Weber-Rendu Syndrome and Intestinal Varices [PDF]
Canadian Journal of Gastroenterology, 1988 A patient with Osler-Weber-Rendu disease and idiopathic intestinal varices who presented with recurrent gastrointestinal hemorrhage and iron deficiency anemia is reported. The unique coexistence of these two rare disorders is discussed and the literature
Robert N. Clark +3 more
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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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Clinical and Biomedical Research, 2013 Homem, 68anos, com história de anemia e episódios frequentes de epistaxe e obstrução nasal pouco responsivos à terapêutica usual, apresentava telangiectasias nas mucosas nasal e oral.
Maurício Farenzena +4 more
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Rendu-Osler-Weber syndrome: A family investigation and review
Journal of Indian Academy of Oral Medicine and Radiology, 2009 Rendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency ...
V G Mahima +3 more
doaj +2 more sources