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Start Over Author "Werner, JA" Language spanish; castilian
2 results on '"Werner, JA"'

1. [Screening for systemic manifestations of vascular malformations in patients with hereditary haemorrhagic telangiectasia (Osler disease)].

Author

Cerra Pohl A, Werner JA, and Folz BJ

Subjects
Brain blood supply, Chromosomes, Human, Pair 2 genetics, Eye blood supply, Humans, Kidney blood supply, Liver blood supply, Lung blood supply, Telangiectasia, Hereditary Hemorrhagic genetics, Vascular Malformations genetics, Mass Screening methods, Telangiectasia, Hereditary Hemorrhagic epidemiology, Telangiectasia, Hereditary Hemorrhagic physiopathology, Vascular Malformations epidemiology, Vascular Malformations physiopathology
Abstract

Hereditary haemorrhagic telangiectasia (Rendu-Osler- Weber syndrome) is a disease characterized by systemic vascular malformations. Typical clinical manifestations are recurrent epistaxis and telangiectases of the skin and the mucous membranes. The syndrome is furthermore characterized by its hereditary aspect. The disease seems to be much more complicated than previously thought, mainly because of the accompanying vascular malformations in vital organs, like the liver, the kidney, the lung, the brain, and the eyes. The diagnosis and treatment of systemic vascular malformations requires interdisciplinary management.

Published
2008

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