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戊二酸血症Ⅰ型的诊治、筛查及产前诊断 被引量:6

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摘要 戊二酸血症Ⅰ型(glutaricacidemia typeⅠ,GA-Ⅰ,OMIM 231670)是一种有机酸血症,因编码戊二酰辅酶A脱氢酶(glutaryl-Co A dehydrogenase,GCDH)的基因突变所致,属于常染色体隐性遗传病^([1])。该疾病的患病率具有种族和地区差异,加拿大部分地区高达1/300,国内报道约为1/60 000^([2])。
出处 《发育医学电子杂志》 2018年第1期20-24,共5页 Journal of Developmental Medicine (Electronic Version)
基金 国家重点研发计划(2016YFC0901505 2016YFC0905100)
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  • 2韩连书,高晓岚,叶军,邱文娟,顾学范.串联质谱分析干血滤纸片酰基肉碱方法的建立[J].中华检验医学杂志,2005,28(1):88-91. 被引量:31
  • 3韩连书,高晓岚,叶军,邱文娟,王瑜,顾学范.串联质谱技术在有机酸血症鉴别诊断中的应用[J].临床儿科杂志,2006,24(12):970-974. 被引量:36
  • 4Feuchtbaum L, Lorey F, Faulkner L, et al. California's experience implementing a pilot newborn supplemental screening program using tandem mass spectrometry. Pediatrics,2006,117 (Suppl) : S261-S269.
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  • 8Chace DH, DiPerna JC, Kalas TA, et al. Rapid diagnosis of methylmalonic and pI;opionic acidemias:quantitative tandem mass spectrometry analysis of propionylcarnitine in filter-paper blood specimens obtained from newborns. Clin Chem,2001,47(11):2040-2044.
  • 9Schmedes A, Brandslund I. Analysis of methylmalonic acid in plasma by liquid chromatography- tandem mass spectrometry. Clin Chemi, 2006,52 (4) :754-757.
  • 10Hasegawa Y, Iga M, Kimura M, et al. Prenatal diagnosis for organic acid disorders using two mass spectrometric methods,gas chromatography mass spectrometry and tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci, 2005,823(1): 13-17.

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