Neurofibromatosis complicated with meningoencephalocele:one case report  

作　　者：HUANG Qi-bing WANG Jian-gang LI Xin-gang ZHOU Xu-dong WANG Dong-hai WANG Xin-yu 

机构地区：[1]Department of Neurosurgery, Qilu Hospital, Shandong University, Ji＇nan 250012, China

出　　处：《Chinese Medical Journal》2007年第23期2151-2152,共2页中华医学杂志（英文版）

摘　　要：Neurofibromatosis type Ⅰ （NF-I） is an autosomal dominant inherited disease caused by a mutated NF-I gene on chromosome 17, which produces inactive neurofibromin. Besides caf6-au-lait spots, and multiple skin neurofibromas,Neurofibromatosis type Ⅰ （NF-I） is an autosomal dominant inherited disease caused by a mutated NF-I gene on chromosome 17, which produces inactive neurofibromin. Besides caf6-au-lait spots, and multiple skin neurofibromas,

关 键 词：neurofibromatosis type Ⅰ orbital meningoencephalocele 

分 类 号：R730.264[医药卫生—肿瘤]