Results 31 to 40 of about 5,408,282 (157)
Journal of Medical Case Reports, 2022 Background Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu disease, induces arteriovenous malformations in visceral organs. Arteriovenous malformations increase the risk of severe infections and are a common complication associated
Genki Naruse +2 more
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Pulmonary arteriovenous malformationsm and follow-up imagings
The Pan African Medical Journal, 2020 An 85-year-old caucasian female with past medical history of hypertension, hyperlipidemia, polymyalgia rheumatica, coronary artery disease, Osler-Weber-Rendu syndrome (diagnosed 18 years ago), intermittent epistaxis and pulmonary arteriovenous ...
Pahnwat Tonya Taweesedt, Salim Surani
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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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Estudio genético de pacientes diagnosticados de enfermedad de Rendu-Osler-Weber (HHT) [PDF]
, 2011 [EN] Although there are previous studies that analyze the Osler Weber Rendu disease in Spanish patients, in our work we intend to analyze from a clinical standpoint and genetic characteristics of patients followed at the Hospital Universitario de ...
Cabezón Crespo, Antonio
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Síndrome de Osler-Weber-Rendu [PDF]
, 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.
Torres, Felipe Soares +4 more
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Computed Tomography Imaging Findings of Hepatic Hereditary Haemorrhagic Telangiectasia [PDF]
Journal of Clinical and Diagnostic Research, 2018 Hereditary Haemorrhagic Telangiectasia (HHT) also known as Osler Weber Rendu disease is a rare, under diagnosed, autosomal dominant multiorgan angio dysplasia.
Nayna Goyal +4 more
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Rendu-Osler-Weber Disease with High Pulmonary Hypertension and Interstitial Lung Disease
Рациональная фармакотерапия в кардиологии, 2023 A 64-year-old female with a family history of hereditary hemorrhagic telangiectasia (HHT) was hospitalized due to complaints of dyspnea during light physical exertion and leg edema. HHT was diagnosed at 20 y.o., recurrent nasal bleeding started at age 52,
Yu. A. Lutokhina +3 more
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Novel mutation in ENG gene causing Hereditary Hemorrhagic Telangiectasia in a Peruvian family [PDF]
Genetics and Molecular Biology, 2020 Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations (AVMs) in multiple organs. Most patients have deletions or missense mutations
Alejandro Zevallos-Morales +9 more
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Thalidomide as an effective treatment in a case of Osler Weber Rendu syndrome: a case report
Asian Journal of Medical Sciences, 2016 Osler Weber Rendu Syndrome (OWRS), or Hereditary Hemorrhagic telangiectasia (HHT) is an autosomal dominant disease presents with epistaxis, telangiactesia and multiorgan vascular dysplasia.
Titli Bandyopadhyay
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A case report of Osler-Weber-Rendu disease with multisystem involvemen
Якутский медицинский журналHereditary hemorrhagic telangiectasia (Osler-Rendu-Weber disease) is a rare disorder with an autosomal dominant inheritance pattern, characterized by small arteriovenous malformations (AVMs) on the mucous membranes and skin (telangiectasias), as well as ...
N. V. Enenkov +2 more
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