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A Case of von Hippel-Lindau Disease with Aortic Valve Insufficiency / 영남의대학술지
Article ي En | WPRIM | ID: wpr-194928
المكتبة المسؤولة: WPRO
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.
الموضوعات
Key words
النص الكامل: 1 الفهرس: WPRIM الموضوع الرئيسي: Aortic Valve / Aortic Valve Insufficiency / Pheochromocytoma / Retinaldehyde / Carcinoma, Renal Cell / Central Nervous System / Hemangioblastoma / Germ-Line Mutation / Hemangioma / Von Hippel-Lindau Disease اللغة: En مجلة: Yeungnam University Journal of Medicine السنة: 2013 نوع: Article
النص الكامل: 1 الفهرس: WPRIM الموضوع الرئيسي: Aortic Valve / Aortic Valve Insufficiency / Pheochromocytoma / Retinaldehyde / Carcinoma, Renal Cell / Central Nervous System / Hemangioblastoma / Germ-Line Mutation / Hemangioma / Von Hippel-Lindau Disease اللغة: En مجلة: Yeungnam University Journal of Medicine السنة: 2013 نوع: Article