Results 101 to 110 of about 411,420 (197)
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
Osler-Weber-Rendu Syndrome, also known as hereditary hemorrhagic telangiectasia, is an autosomal dominant disease characterized by the presence of vascular telangiectasias in the skin and mucosa.
Tarhan, Mustafa Oktay
core +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
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
, 2010 We report a symptomatic newborn with Osler-Rendu-Weber syndrome, multiple and diffuse pulmonary arteriovenous malformations, and right-to-left shunting in the left lung.
Ruf, B;Eicken, A;Schreiber, C;Hess, J
core +1 more source
Severe osteomalacia with multiple insufficiency fractures secondary to intravenous iron therapy in a patient with Rendu-Osler-Weber syndrome. [PDF]
Bone Rep, 2020 Callejas-Moraga EL +3 more
europepmc +1 more source
Revista Finlay, 2015 Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder of the walls of the blood vessels that become tortuous and dilated. Clinically, patients with this disease develop recurrent bleeding, which may occur spontaneously or following ...
Rodolfo Morales Valdés +5 more
doaj +2 more sources
Revista Cubana de Hematología, Inmunología y Hemoterapia, 2012 Los pacientes con epístaxis representan entre el 10 y 12 % de los casos atendidos en los servicios de urgencia de otorrinolaringología. Se presentan 5 pacientes atendidos en este servicio del Hospital General Docente "Enrique Cabrera", en el período ...
Tahamara Alcalá-Villalón +2 more
doaj
A Case of Osler-Weber-Rendu Syndrome Complicated with Nasal Septum Perforation
, 2020 Objectives: Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is a rare autosomal dominant disorder characterized by multiple mucocutaneous telangiectasias and visceral arteriovenous malformations.
Jukhai, Layala +4 more
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