Osler-Weber-Rendu syndrome: a case report with familial clustering.
Indian J Dermatol Venereol Leprol
;
2009 Jan-Feb; 75(1): 100-1
Artículo
en Inglés
| IMSEAR
| ID: sea-53037
ABSTRACT
Osler-Weber-Rendu syndrome, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant disorder manifested by telangiectases of the skin and mucous membranes and arteriovenous malformations of various organ systems. We present a case of Osler-Weber-Rendu syndrome with 11 affected members in her family.
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IMSEAR (Asia Sudoriental)
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Inglés
Revista:
Indian J Dermatol Venereol Leprol
Año:
2009
Tipo del documento:
Artículo
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