戊二酸尿症Ⅰ型的研究进展
摘要
戊二酸尿症Ⅰ型(GI)为常染色体隐性遗传疾病,1975年由Goodman等首次报道。多个国家将该病作为新生儿筛查疾病,国外报道新生儿患病率约为1/100000。国内对此疾病的认识尚不足,因其非特异性临床表现易致漏诊误诊。国内尚未开展该病的新生儿筛查,发生率无多中心的统计数据。浙江省新生儿筛查发病率为1/64708。
出处
《中华儿科杂志》
CAS
CSCD
北大核心
2012年第12期912-914,共3页
Chinese Journal of Pediatrics
基金
国家自然科学基金(81070699)
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共引文献72
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1谭建强,陈大宇,严提珍,黄钧,蔡稔.三例戊二酸血症Ⅰ型患儿的临床特点及GCDH基因变异分析[J].中华医学遗传学杂志,2019,36(9):882-885. 被引量:1
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2李育霖,孙萌,李盼盼,田丽萍,郭元芳,李改杰,李若彤,闫妍,李青,邹卉.新生儿甲基丙二酸血症生化筛查与基因筛查结果分析[J].中华实用儿科临床杂志,2023,38(1):54-59. 被引量:6
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