CAJ | 학술논문

结合文献对本院2006年5月至2009年11月经头颅MRI诊断为丹迪-沃克综合征的5例患者的临床资料进行分析.结果显示,该病临床特点以运动发育迟缓和小脑体征多见,5例中3例伴有小脑体征.多在儿童期发病.头颅影像学检查表现为第四脑室扩大,小脑蚓部体积变小或缺如.MRI是诊断丹迪-沃克综合征的最佳辅助检查方法.
결합문헌대본원2006년5월지2009년11월경두로MRI진단위단적-옥극종합정적5례환자적림상자료진행분석.결과 현시,해병림상특점이운동발육지완화소뇌체정다견,5례중3례반유소뇌체정.다재인동기발병.두로영상학검사표현위제사뇌실확대,소뇌인부체적변소혹결여.MRI시진단단적-옥극종합정적최가보조검사방법.
5 cases diagnosed with Dandy-Walker Syndrome from May 2006 to November 2009 were investigated and relevant literature reviewed. Dandy-Walker Syndrome was characterized by retarded motordevelopment and cerebellar signs. The latter was observed in 3 cases in our series. The disorder, mostly influencing childhood, typically causes the fourth ventricle enlarged, and the cauda cerebelli atrophic or even absent. MRI is the most optimal radiological method to diagnose it.