Results 31 to 40 of about 411,420 (197)

Syndrome in Question [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2014
Rendu-Osler-Weber Syndrome also known as Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia, with dominant autosomal inheritance.
Sheila Itamara Ferreira do Couto Meireles   +4 more
doaj   +1 more source

Rendu-Osler-Weber Disease [PDF]

open access: yesCirculation, 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

Rheumatoid arthritis associated with Rendu — Osler — Weber disease: Second description [PDF]

open access: yes, 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

Estudio genético de pacientes diagnosticados de enfermedad de Rendu-Osler-Weber (HHT) [PDF]

open access: yes, 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
core   +1 more source

Pulmonary arteriovenous malformation

open access: yesJournal 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]

open access: yesModern Medicine
Introduction 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]

open access: yes, 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
core   +1 more source

Hereditary Hemorrhagic Telangiectasia

open access: yesPediatric 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
doaj   +1 more source

Epistaxis Runs in the Family

open access: yesOman 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
doaj   +1 more source

Patient with anaemia and Rendu-osler-weber syndrome [PDF]

open access: yesRevista 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
openaire   +1 more source

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