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Screening Mentally Retarded Children for Inborn Errors of Metabolism

机译:筛选智障儿童的先天性代谢错误

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Background: Most inborn errors of metabolism result in mental retardation and death due to accumulation of abnormal metabolites in the tissues. The presence of abnormal metabolites in the urine of mentally retarded individuals has been used worldwide for detection of inborn errors of metabolism. The purpose of the study is to determine the prevalence of inborn error of metabolism in mentally retarded children. Methods: Random urine samples were collected from mentally retarded children at two institutes in Kathmandu, and also from 60 normal children from Duwakot, Nepal after obtaining consent from their parents. Urine was then tested for the presence of amino acids, keto-acids, mucopolysaccharides, fructose, glucose and protein using simple qualitative color reactions in the laboratory. Results: The tests detected eight cases of Phenylketonuria, which turned out to be false positive on paper chromatography. Three cases of presence of ketone bodies (acetoacetate), ten cases of α-ketoaciduria, two cases of mucopolysaccharidosis and twelve cases of fructosuria amongst the sixty-two urine samples were also found. Conclusions: Certain aminoacidurias, ketoacidurias and mucopolysaccharidoses might be present in the Nepalese population. Within consideration of errors, the samples tested positive should be evaluated by a higher end method to confirm the utility of these simple and cheap chemical tests. ?
机译:背景:大多数先天性代谢错误会由于组织中异常代谢产物的积累而导致智力低下和死亡。智障者尿液中异常代谢产物的存在已被全世界用于检测先天性代谢错误。这项研究的目的是确定弱智儿童先天性代谢错误的发生率。方法:在获得父母同意后,从加德满都两家机构的智障儿童以及尼泊尔杜瓦科特的60名正常儿童中随机抽取尿液样本。然后在实验室中使用简单的定性颜色反应测试尿液中氨基酸,酮酸,粘多糖,果糖,葡萄糖和蛋白质的存在。结果:该测试检测到八例苯丙酮尿症,在纸色谱法上证明是假阳性。在62份尿液样本中,还发现了3例存在酮体(乙酰乙酸),10例α-酮酸尿,2例粘多糖贮积症和12例果尿尿。结论:尼泊尔人群中可能存在某些氨基酸尿症,酮症尿酸症和粘多糖贮积酶。在考虑误差的情况下,应采用更高端的方法评估测试阳性的样品,以确认这些简单而廉价的化学测试的实用性。 ?

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