Results 51 to 60 of about 583,024 (194)
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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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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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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Endoscopic Classification of Severe Spontaneous Epistaxis: A Case‐Series of 445 Patients
Laryngoscope Investigative Otolaryngology, Volume 11, Issue 2, April 2026.Epistaxis can be related to several histopathological findings. ABSTRACT Objective To identify the anatomical location and characterize the histopathological findings of severe spontaneous epistaxis through endoscopic evaluation and tissue biopsy.
Wen Zhang +2 more
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Fibrodysplastic implications for transvenous embolization of a high-flow pelvic arteriovenous malformation in Osler-Weber-Rendu syndrome [PDF]
, 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
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Enfermedad de Rendu Osler Weber: presentación de un caso
Galicia Clínica, 2021 La Telangiectasia Hemorrágica Hereditaria o Enfermedad de Rendu-Osler- Weber, es una entidad infradiagnosticada y el retraso diagnóstico es fre- cuente, lo que va a difi el screening y tratamiento preventivo de los pacientes y de sus familiares afectos ...
Ana Arévalo Gómez +3 more
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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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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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Ischemic cholangitis during Osler-Weber-Rendu disease: a case report
Egyptian Liver Journal, 2022 Background Osler-Weber-Rendu disease (OWRD) is a rare autosomal dominant genetic disease that causes skin and mucosal telangiectasias and visceral arteriovenous malformations.
Oussama Kharmach +4 more
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