Osler-Weber-Rendu disease (OWRD) is a rare autosomal dominant disorder that affects blood vessels throughout the body (causing vascular. Download Citation on ResearchGate | Telangiectasia hemorrágica hereditaria Enfermedad de Osler Weber Rendu | Hereditary hemorrhagic telangiectasia. Telangiectasia hemorrágica hereditaria: enfermedad de Rendu-Osler-Weber. Article in FMC – Formación Médica Continuada en Atención.

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Diagnosis can be based on clinical signs such enfdrmedad upper respiratory tract changes or recurrent hemorrhagic events. Nevertheless, pulmonary involvement, a prognostic factor, may remain undetected.

Arteriography demonstrated a single PAVM in one case and the patient underwent successful coil embolization, with clinical and functional improvement.

A report of three cases.

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Universidad de Buenos Aires. Nevertheless, pulmonary involvement, a prognostic factor, may remain undetected. Arteriography demonstrated a single PAVM in one case and the patient underwent successful coil embolization, with clinical and functional improvement.

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Thorax, 54pp. Am Rev Respir Weberr,pp.

Rendu-Osler-Weber Syndrome: case report and literature review

A state of the art review. Two-dimensional contrast echocardiography in the detection and follow-up of congenital pulmonary arteriovenous malformations. Am J Cardiol, 68pp.

Radiology,pp. Angioarchitecture of pulmonary arteriovenous malformations: Clinical utility of three- dimensional helicoidal CT. N Engl J Med,pp.

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemmorrhagic telangiectasia. Embolotherapy of large pulmonary arteriovenous malformations: Ann Thorac Surg, 64pp. Malformaciones arteriovenosas pulmonares y complicaciones Si engermedad navegando, consideramos que acepta su uso.

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