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无脑回畸形儿1例报告并文献复习

Lissencephaly: a case report and literature review

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【作者】 江军李承赵培伟何学莲

【Author】 JIANG Jun;LI Cheng;ZHAO Peiwei;HE Xuelian;Department of Electrophysiology, Wuhan Children’s Hospital;Clinical Research Center, Wuhan Children’s Hospital;

【机构】 武汉市儿童医院神经电生理室武汉市儿童医院中心实验室

【摘要】 目的探讨无脑回畸形的临床特征及其致病基因LIS1基因的检测特点。方法回顾性分析1例无脑回畸形患儿的临床、实验室检查及基因检测结果,同时复习相关文献。结果女性,5月龄,确诊癫痫20 d,3 d内再次抽搐发作30余次入院,抽搐发作表现为双眼凝视、上翻,口唇、面色发绀,口吐白沫,四肢强直,意识丧失,约2~3 min自行缓解。外周血白细胞计数13.67×109/L,血红蛋白108 g/L,红细胞计数3.90×1012/L,淋巴细胞10.26×109/L;心肌酶谱、肝肾功能均正常;血氨23μmol/L,乳酸2.11 mmol/L;长程视频脑电图显示高度失律,频繁部分性发作,有时继发全身阵挛发作。头部MRI提示无脑回畸形。口服左乙拉西坦片,约27 mg/(kg·d),托吡酯片约6.5 mg/(kg·d),目前暂无发作。患儿LIS1基因检测发现c.232del G杂合突变,导致蛋白移码突变(p.E78Nfs X25);患儿父母均未见突变。结论无脑回畸形患儿可合并癫痫,可能由LIS1基因突变所致,该基因c.232del G位点突变在国内外未见报道。

【Abstract】 Objective To explore the clinical features of lissencephaly and the detection of LISI gene. Methods The characteristic of clinical features, laboratory examination and gene detection in one case of lissencephaly was retrospectively analyzed. Meanwhile, the related literatures were reviewed. Results A 5-month-old female child diagnosed with epilepsy 20 days ago was hospitalized for convulsive seizure more than 30 times in 3 days. The manifestations were eyes staring, and turning upward, cyanosis of lips and face, froth at the mouth, extremities rigidity and loss of consciousness, and the symptoms can spontaneously remitted in 2-3 minutes. Laboratory examination showed that peripheral blood white cell count was 13.67×109/L, hemoglobin 108 g/L, red blood cell count 3.90×1012/L, lymphocyte 10.26×109/L; maocardial enzyme and hepatic and renal function were normal; blood ammonia was 23 μmol/L and lactic acid 2.11 mmol/L. Long-range video EEG showed highly arrhythmia, and frequent partial epilepsy, and sometimes secondary generalized epilepsy. Head MRI showed lissencephaly. The child was treated with oral administration of Keppra 27 mg/(kg·day), Topiramate 6.5 mg/(kg·day), currently no seizure. The detection of LIS1 gene found that heterozygous mutation of c.232 del G, which lead to protein shift mutation(p.E78 Nfs X25). No mutation was found in her parents. Conclusions Child with lissencephaly may combine with epilepsy which may cause by mutation in LIS1 gene. And there was no information about point mutation of c.232 del G in LIS1 gene being reported at home and abroad so far.

【关键词】 无脑回畸形LIS1基因基因检测
【Key words】 lissencephalyLIS1 genegene detection
【基金】 武汉市科技创新平台-儿童神经疾病临床医学研究中心资助项目(No.2014-160)
  • 【文献出处】 临床儿科杂志 ,Journal of Clinical Pediatrics , 编辑部邮箱 ,2016年06期
  • 【分类号】R742
  • 【下载频次】130
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