A Case of von Hippel-Lindau Disease with Aortic Valve Insufficiency / 영남의대학술지
Yeungnam University Journal of Medicine
;
: 101-104, 2013.
Article
Dans Anglais
| WPRIM
| ID: wpr-194928
ABSTRACT
Von Hippel-Lindau (VHL) disease is an autosomal dominant hereditary disorder caused by a germline mutation of the VHL gene. It is a multi-systemic disorder that is predisposed to benign or malignant tumors of visceral organs such as hemangioblastoma of the central nervous system, renal cell carcinoma, retinal angioma and pheochromocytoma. We report herein a case of VHL disease that initially manifested with aortic valve insufficiency.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Valve aortique
/
Insuffisance aortique
/
Phéochromocytome
/
Rétinal
/
Néphrocarcinome
/
Système nerveux central
/
Hémangioblastome
/
Mutation germinale
/
Hémangiome
/
Maladie de von Hippel-Lindau
langue:
Anglais
Texte intégral:
Yeungnam University Journal of Medicine
Année:
2013
Type:
Article
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