[1]刘 龙,李力仙.Chiari畸形Ⅰ型发病机制研究进展[J].新乡医学院学报,2016,33(4):325-328.[doi:10.7683/xxyxyxb.2016.04.020]
 LIU Long,LI Lixian.Research progress of the pathogenesis of Chiari malformation type I[J].Journal of Xinxiang Medical University,2016,33(4):325-328.[doi:10.7683/xxyxyxb.2016.04.020]
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Chiari畸形Ⅰ型发病机制研究进展
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《新乡医学院学报》[ISSN:1004-7239/CN:41-1186/R]

卷:
33
期数:
2016年4
页码:
325-328
栏目:
综述
出版日期:
2016-04-06

文章信息/Info

Title:
Research progress of the pathogenesis of Chiari malformation type I
作者:
刘 龙李力仙
(哈尔滨医科大学附属第一医院神经外科,黑龙江 哈尔滨 150001)
Author(s):
LIU LongLI Lixian
关键词:
Chiari畸形Ⅰ型脊髓空洞症发病机制细胞学分子学胚胎学
分类号:
R651
DOI:
10.7683/xxyxyxb.2016.04.020
文献标志码:
A
摘要:
Chiari畸形Ⅰ型是一种先天性疾病,常伴有脊髓空洞症,形成机制复杂,目前尚无定论。本文从细胞学、分子学和胚胎学等不同方面对Chiari畸形Ⅰ型的发病机制进行梳理,同时,对其并发脊髓空洞症的机制进行概述,为Chiari畸形Ⅰ型及其合并脊髓空洞症的临床诊断、治疗提供参考。

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更新日期/Last Update: 2016-04-05