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TH基因变异致婴儿多巴反应性肌张力障碍4例临床和基因分析
引用本文:胡恕香,黄燕茹,李培,蔡慧强,李文洁,彭桂兰. TH基因变异致婴儿多巴反应性肌张力障碍4例临床和基因分析[J]. 临床儿科杂志, 2021, 39(3): 191-195. DOI: 10.3969/j.issn.1000-3606.2021.03.007
作者姓名:胡恕香  黄燕茹  李培  蔡慧强  李文洁  彭桂兰
作者单位:厦门大学附属妇女儿童医院儿童神经康复科 福建厦门 361003;厦门大学附属妇女儿童医院中心实验室 福建厦门 361003
摘    要:
目的 探讨婴儿起病的多巴反应性肌张力障碍(DRD)的临床及遗传特征.方法 回顾分析2016年4月—2020年6月收治的4例婴儿期起病的DRD患儿的临床资料.结果 4例患儿中,男性3例、女性1例,起病年龄2~7个月.临床表现为发育落后或发育倒退,肌无力,肌张力障碍.患儿血生化、血氨、血乳酸无异常;脑电图、头颅磁共振成像(...

关 键 词:Segawa病  多巴胺  肌张力障碍  TH基因

Clinical and genetic analysis of dopa-responsive dystonia caused by compound heterozygous mutation of TH gene in 4 infants
HU Shuxiang,HUANG Yanru,LI Pei,CAI Huiqiang,LI Wenjie,PENG Guilan. Clinical and genetic analysis of dopa-responsive dystonia caused by compound heterozygous mutation of TH gene in 4 infants[J]. The Journal of Clinical Pediatrics, 2021, 39(3): 191-195. DOI: 10.3969/j.issn.1000-3606.2021.03.007
Authors:HU Shuxiang  HUANG Yanru  LI Pei  CAI Huiqiang  LI Wenjie  PENG Guilan
Affiliation:1 .Department of Pediatric Psychiatric Rehabilitation; 2 .Department of Genetic Diagnosis Center, Women and Children’s Hospital, School of Medicine, Xiamen University, Xiamen 361003 , Fujian, China
Abstract:
Objective To explore the clinical and genetic characteristics of dopa-responsive dystonia(DRD)in infants.Methods The clinical data of DRD in 4 infants admitted from April 2016 to June 2020 were retrospectively analyzed.Results In the 4 children(3 boys and 1 girl)the onset age ranged from 2 months to 7 months.The clinical manifestations were developmental retardation or regression,muscle weakness and dystonia.There were no abnormalities in blood biochemistry,blood ammonia and blood lactic acid tests.Electroencephalogram and cranial magnetic resonance imaging(MRI)showed no obvious abnormality.There was no abnormality in routine chromosomal examination,while the compound heterozygous pathogenic variation of TH gene was found.In case 1,c.457 C>T was inherited from the father and c.1196C>T was inherited from the mother.In case 2,c.698G>A was inherited from the father and c.1293+5G>C was inherited from the mother.In case 3,c.880 G>C was inherited from father and c.690 C>A was inherited from the mother.In case 4,c.739 G>A was inherited from the father and c.1293+5 G>C was inherited from the mother.All of them were reported to be pathogenic variants.Cases 1,2,and 3 were treated with low dose of dopasrazide after diagnosis,and the dose was gradually increased to obtain the best effect.The children were followed up for 1.5~3 years,and the current maximum dose of the drug was 20~25 mg/(kg·d).All the children recovered basically.At present,the dosage of dosilazine in case 4 was 12 mg/(kg·d),and dystonia was still present when agitated,and the dosage was continued to be increased slowly.Conclusion The symptoms of DRD are not special in infants.Genetic tests should be performed as soon as possible,and the treatment effect of doserazine is good.
Keywords:Segawa disease  dopamine  dystonia  TH gene
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