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通过尿酰基甘氨酸的稳定同位素稀释分析诊断中链酰基辅酶A脱氢酶缺乏症:回顾性和前瞻性研究,以及将其准确性与通过快原子轰击/质谱法鉴定酰基肉碱进行比较

Diagnosis of medium chain acyl-CoA dehydrogenase deficiency by stable isotope dilution analysis of urinary acylglycines: retrospective and prospective studies, and comparison of its accuracy to acylcarnitine identification by FAB/mass spectrometry.

作者信息

Rinaldo P, O'Shea J J, Welch R D, Tanaka K

机构信息

Yale University School of Medicine, Department of Human Genetics, New Haven, CT 06510.

出版信息

Prog Clin Biol Res. 1990;321:411-8.

PMID:2326302
Abstract

In summary, we have demonstrated that the accurate quantitation of urinary HG and PPG by stable isotope dilution analysis is currently the most reliable method for the diagnosis of MCAD deficiency. This method is particularly useful for testing random samples from asymptomatic patients without any provocative test, and it is suitable to widely survey a fairly large population, such as patients with episodic manifestations and families with a history of SIDS.

摘要

总之,我们已经证明,通过稳定同位素稀释分析对尿中己二酸和戊二酸进行准确定量,是目前诊断中链酰基辅酶A脱氢酶缺乏症最可靠的方法。该方法对于检测无症状患者的随机样本而无需任何激发试验特别有用,并且适用于对相当大的人群进行广泛调查,例如有发作性表现的患者和有婴儿猝死综合征病史的家庭。

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