Results 41 to 50 of about 583,024 (194)
Rendu-Osler-Weber Disease [PDF]
Circulation, 2001 A 75-year-old man was admitted to the hospital because of transient unconsciousness and dysarthria. Brain CT and MRI demonstrated a recent cerebellar infarction. Physical examination revealed a continuous extracardiac murmur maximally auscultated (Levine III) between the inner edge of the right scapula and the upper thoracic vertebrae.
H, Kataoka, O, Matsuno
openaire +2 more sources
Osler-Weber-Rendu Syndrome: A Case Report With Familial Clustering [PDF]
, 2009 Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems.
Sahni, H. +5 more
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Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT-Like Syndromes: A Comparative Overview. [PDF]
Eur J NeurolHereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Palermo M, Sturiale CL.
europepmc +2 more sources
Síndrome de Osler Weber Rendau en adulto mayor [PDF]
, 2022 Objective: To expose the main clinical characteristics to make the diagnosis of Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome. Case presentation: We present the case of a 70-year-old patient with a history of repeated epistaxis who ...
Esteban Badillo, Laura Yibeth +4 more
core +1 more source
Patient with anaemia and Rendu-osler-weber syndrome [PDF]
Revista Andaluza de Patología Digestiva, 2021 Resumen Varón de 66 años con Telangiectasia Hemorrágica Hereditaria tipo I que consulta por astenia intensa detectándose en analítica Hb 4 mg/dl; VCM 100,5%. El paciente no refiere síntomas de sangrado. En gastroscopia se visualizan múltiples malformaciones vasculares de tamaño variable y sin sangrado activo en esófago, estómago, siendo más ...
A Roa Colomo +2 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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Rheumatoid arthritis associated with Rendu — Osler — Weber disease: Second description [PDF]
, 2021 The article presents second ever published description of rheumatoid arthritis case co-morbid with Rendu — Osler — Weber disease (hereditary hemorrhagic teleangiectasia) in a 63-yearsold female patient.
de Carvalho, Jozélio Freire +3 more
core +1 more source
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
doaj +1 more source
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
doaj +1 more source
Osler-Weber-Rendu Syndrome [PDF]
, 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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