von Hippel-Lindau Disease A Case Series of Unusual Familial Cancer Syndrome

被引：1

作者：

Ganesh, H. K. ^{[1
]}

Gopal, Raju A. ^{[1
]}

George, Joe ^{[1
]}

Bandgar, Tushar ^{[1
]}

Menon, Padma ^{[1
]}

Shah, Nalini ^{[1
]}

机构：

[1] King Edward Mem Hosp, Dept Endocrinol, Bombay 400012, Maharashtra, India

来源：

ENDOCRINOLOGIST | 2010年 / 20卷 / 03期

关键词：

von Hippel-Lindau (VHL); pheochromocytoma; pancreatic cyst; FEATURES;

D O I：

10.1097/TEN.0b013e3181dfdc98

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

von Hippel-Lindau (VHL) disease is a familial cancer syndrome inherited in an autosomal dominant manner, caused by mutations in the VHL tumor suppressor gene. We report 7 cases of VHL, evaluated in our hospital.

引用

页码：134 / 136

页数：3

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