首页> 外文期刊>Journal of inherited metabolic disease >Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile.
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Carnitine palmitoyltransferase I deficiency in neonate identified by dried blood spot free carnitine and acylcarnitine profile.

机译:肉碱棕榈酰转移酶I缺乏症通过干血点无肉碱和酰基肉碱分布来确定。

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摘要

A neonate at risk for hepatic carnitine palmitoyltransferase I (L-CPT I) deficiency was investigated from birth. The free carnitine and acylcarnitine profile in dried whole blood filter paper samples collected at ages 1 and 4 days showed a markedly elevated concentration of free carnitine (141 and 142 micromol/L, respectively), normal concentrations of acetyl- and propionylcarnitine, with the near absence of all other species. The diagnosis was confirmed by in vitro fatty acid oxidation screening assays and enzyme assay in cultured skin fibroblasts. Retrospective study of the newborn whole blood sample of the index case showed a similar profile (free carnitine 181 micromol/L). The newborn population distribution of free carnitine (n = 143,981) showed that only three samples had free carnitine > 140 micromol/L (>99.9th centile), two were from L-CPT I-deficient neonates and one from a baby with sepsis. While there are other conditions that can cause elevated concentrations of free carnitine, an isolated elevation of free carnitine only in an apparently healthy term neonate warrants further investigation to exclude L-CPT I deficiency.
机译:从出生开始就调查了有肝肉碱棕榈酰转移酶I(L-CPT I)缺乏症风险的新生儿。在第1天和第4天采集的干燥全血滤纸样品中的游离肉碱和酰基肉碱分布表明,游离肉碱浓度显着升高(分别为141和142 micromol / L),乙酰基和丙酰基肉碱的正常浓度接近没有其他所有物种。通过体外脂肪酸氧化筛选测定和培养的皮肤成纤维细胞中的酶测定证实了该诊断。对指标病例的新生儿全血样本的回顾性研究显示出相似的特征(游离肉碱181 micromol / L)。新生儿游离肉碱的分布(n = 143,981)显示,只有三个样品的游离肉碱> 140 micromol / L(> 99.9个百分位数),两个样品来自L-CPT I缺陷型新生儿,一个来自败血症婴儿。尽管还有其他条件可能导致游离肉碱浓度升高,但仅在表面健康的新生儿中游离肉碱的孤立升高值得进一步研究以排除L-CPT I缺乏症。

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