[Rendu-Osler-Weber disease as an infrequent cause of stroke].
Revista de neurologia, 2008 Hereditary haemorrhagic telangiectasia, or Rendu-Osler disease, is a congenital vascular disease that is associated with the presence of arteriovenous fistulas that cause paradoxical embolisms.An 83-year-old female with clinical signs and symptoms of convulsive attacks and multiple cerebral infarctions in the acute phase.
Mas-Sese G +5 more
openaire +3 more sources
Osler Weber Rendu Disease ( A Case Report)
Eurasian Journal of Medicine, 2019 -
Nihat Okçu +3 more
doaj
Fístula arteriovenosa de la circulación pulmonar: Relación con la enfermedad de Rendu - Osler - Weber. A propósito de 14 observaciones [PDF]
, 1979 The arteriovenous fistula in lung is a rare condition. The paper contains a review of main clinical characteristics, radiological examinations and other tests which render diagnosis easy, performed on a series of 14 patients.The authors then proceed to ...
Muras, Olga +2 more
core +1 more source
Hæmorrhagic Telangiectasia of Rendu-Osler-Weber [PDF]
Proceedings of the Royal Society of Medicine, 1946 openaire +3 more sources
Fístula arteriovenosa de la circulación pulmonar
Cirugía del Uruguay, 1979 La fístula arteriovenosa pulmonar es una afección poco frecuente. A propósito de 14 observaciones reseñamos las principales características clínicas así como exámenes radiológicos y otros que permiten un fácil diagnóstico.
Olga Muras +2 more
doaj
[Cerebral ischemia in Rendu-Osler-Weber disease].
Neurologia (Barcelona, Spain), 2000 Neurologic manifestations occur in 8-12% of the patients with Rendu-Osler-Weber disease or hereditary hemorrhagic telangiectasia (HHT), principally infectious and hemorrhagic and, less frequently, ischemic ones. More than a half of these neurologic complications are associated with pulmonary arterio-venous malformations (PAVM).
S, Delgado Reyes +5 more
openaire +1 more source
Life-threatening Anaemia in Patient with Hereditary Haemorrhagic Telangiectasia (Rendu-Osler-Weber Syndrome). [PDF]
Open Med (Wars), 2020 Mikołajczyk-Solińska M +4 more
europepmc +1 more source
[A visceral form of Rendu-Osler-Weber syndrome].
Terapevticheskii arkhiv, 1985 A case of a visceral pattern (with primary liver injury) of the Rendu-Osler-Weber disease is described with emphasis on the diagnostic difficulties due to the absence of external symptoms of disease and hemorrhage. Stress is laid on the importance of making liver biopsy in the diagnosis of this pattern of teleangioectatic disease.
A S, Loginov +4 more
openaire +1 more source
Hereditary hemorrhagic telangiectasia, liver disease and elevated serum testosterone (Osler–Weber–Rendu syndrome): a case report [PDF]
, 2017 core +1 more source
A case report of recurrent acute ischemic strokes in a young patient with Rendu-Osler-Weber disease [PDF]
, 2018 Rendu-Osler-Weber disease is a rare inherited disease of the vasculature, characterized by the development of multiple telangiectasias of the skin and mucous membranes, as well as hemorrhagic syndrome of various localization.
Chernukha, T. N. +11 more
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