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D-甘油酸血症:一种新综合征的生化研究

D-glyceric acidemia: biohcemical studies of a new syndrome.

作者信息

Kolvraa S, Rasmussen K, Brandt N J

出版信息

Pediatr Res. 1976 Oct;10(10):825-30. doi: 10.1203/00006450-197610000-00003.

Abstract

Studies of a mentally retarded boy, clinically suffering from nonketotic hyperglycinemia, are reported. Using combined gas chromatography-mass spectrometry, enzyme specificity studies, and spectropolariometry D-glyceric acid in extremely elevated concentrations was demonstrated in both serum and urine (serum: 1.0-1.3 mmol/liter, urine: 33-187 mmol/liter). Hydroxypyruvic acid was not detectable in urine from this boy using a gas chromatographic method with a limit of detection of 0.3 mmol/liter. Enzyme assays of D-glyceric dehydrogenase on blood leukocytes demonstrated significantly lower activity in the patient compared with five normal children.

摘要

报告了对一名临床上患有非酮症高甘氨酸血症的智障男孩的研究。采用气相色谱 - 质谱联用、酶特异性研究和旋光测定法,在血清和尿液中均检测到浓度极高的D - 甘油酸(血清:1.0 - 1.3毫摩尔/升,尿液:33 - 187毫摩尔/升)。使用检测限为0.3毫摩尔/升的气相色谱法,在该男孩的尿液中未检测到羟基丙酮酸。对患者血液白细胞进行的D - 甘油酸脱氢酶酶活性测定表明,与五名正常儿童相比,患者的活性显著降低。

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