首页> 外国专利> DIAGNOSTIC TECHNIQUE IN CHILDREN OF ASTHENIC-VEGETATIVE SYNDROME UNDER EXPOSURE CONDITIONS WITH ALUMINUM

DIAGNOSTIC TECHNIQUE IN CHILDREN OF ASTHENIC-VEGETATIVE SYNDROME UNDER EXPOSURE CONDITIONS WITH ALUMINUM

机译:铝暴露条件下体虚综合症患儿的诊断技术

摘要

FIELD: medicine.;SUBSTANCE: what is presented is a diagnostic technique in children of asthenic-vegetative syndrome under conditions of aluminum exposure. Content of aluminum is determined in urine sample of child. DNA is extracted from buccal epithelium sample. Then, genotyping of polymorphism of genotypes of glutamate ion receptor GRIA1 (rs545098) and glial glutamate transporter gene SLC2A1 (rs841839) is carried out on a detecting polymerizer using real-time polymerase chain reaction. If observing the following conditions simultaneously: availability of variant homozygous or heterozygous genotypes of GRIA1 gene (rs545098) and SLC2A1 gene (rs841839), under the condition of simultaneous detection in the patient of excess content of aluminum in urine in more than 1.3 times as compared to the reference, the presence of asthenic-vegetative syndrome in conditions of aluminum exposure is diagnosed in a child.;EFFECT: invention provides reliable establishment at an early stage of assessing the effect of aluminum on the onset of asthenic-vegetative syndrome by using an aggregate of genetic markers and aluminum content in urine as an informative criterion.;1 cl, 2 tbl, 2 ex
机译:领域:药物;物质:提出了一种在铝暴露条件下对儿童缺乏营养的综合症的诊断技术。铝的含量在儿童的尿液样本中确定。从颊上皮样品中提取DNA。然后,使用实时聚合酶链反应在检测聚合器上进行谷氨酸离子受体GRIA1(rs545098)和神经胶质谷氨酸转运蛋白基因SLC2A1(rs841839)的基因型多态性的基因分型。如果同时观察以下情况:在同时检测到患者尿液中铝含量超过1.3倍的条件下,GRIA1基因(rs545098)和SLC2A1基因(rs841839)的纯合或杂合基因型变异型的可用性作为参考,可以诊断出在儿童中铝暴露情况下是否存在衰弱-植物性综合症。效果:本发明提供了可靠的证据,可以通过评估使用铝在早期评估铝对衰弱-植物性综合症发作的影响。尿液中的遗传标志物和铝含量的总和作为参考标准; 1 cl,2 tbl,2 ex

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