期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
Status epilepticus associated with Mycoplasma pneumoniae encephalitis in children: good prognosis following early diagnosis and treatment 被引量:4
1
作者 Shuo Feng jin-Xiao Chen +7 位作者 Ping Zheng jian-Zhao Zhang Zhi-jie Gao Ying-Ying Mao xin-na ji Shu-Hua Chen Hong-Mei Sun Qian Chen 《Chinese Medical Journal》 SCIE CAS CSCD 2019年第12期1494-1496,共3页
Mycoplasma pneumoniae is a common pathogen that leads to respiratory tract infections in children, often causing immune-related injuries in multiple other organs and tissues. The involvement of central nervous system ... Mycoplasma pneumoniae is a common pathogen that leads to respiratory tract infections in children, often causing immune-related injuries in multiple other organs and tissues. The involvement of central nervous system has been reported in 5% to 7% of patients with M. pneumoniae infection.[1] The clinical manifestations of M. pneumoniae encephalitis are highly heterogeneous, and more than half of patients experience seizures during the acute phase, with status epilepticus occurring in severe cases.[2] 展开更多
关键词 Status epilepticus MYCOPLASMA PNEUMONIAE ENCEPHALITIS PROGNOSIS
原文传递
A Novel WDR45 Mutation in a 9-Month-Old Male Infant with Epileptic Spasms
2
作者 Wan-Ting Liu Qian Chen +3 位作者 Zhi-jie Gao xin-na ji Ke-Ming Xu Yan-Yan Cao 《Chinese Medical Journal》 SCIE CAS CSCD 2018年第24期2991-2992,共2页
To the Editor:Neurodegeneration with brain iron accumulation (NBIA)comprises a group of disorders that manifest as early-or late-onset parkinsonism,dystonia,spasticity,and cognitive impairment, One subtype of NBIA,β-... To the Editor:Neurodegeneration with brain iron accumulation (NBIA)comprises a group of disorders that manifest as early-or late-onset parkinsonism,dystonia,spasticity,and cognitive impairment, One subtype of NBIA,β-propeller protein-associated neurodegeneration (BPAN),is caused by mutation of the WDR45 gene.To date,59 novel WDR45 mutations have been reported.The literature indicates that it is difficult to detect the disorder in early childhood because no specific clinical or imaging features exist. In this report,we describe the case of a 9-month-old male Chinese infant with a novel mutation (c.977-1 C >T)in the WDR45 gene. 展开更多
关键词 WDR45 MUTATION MALE INFANT Epileptic SPASMS
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部