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METHOD FOR DETERMINING RISK OF DEVELOPING EXFOLIATION SYNDROME OR EXFOLIATION GLAUCOMA

机译:确定发展为剥脱性综合征或剥脱性青光眼的风险的方法

摘要

A method for assisting the diagnosis of the risk of developing exfoliation syndrome or exfoliation glaucoma in a subject, said method comprising: an allele measurement step of measuring alleles for at least 30 single nucleotide polymorphisms (SNPs) including the 12 core SNPs listed in Table 1 and SNPs selected from the pool SNPs listed in Table 2 (selected pool SNPs), on the basis of SNP allele information in a biological sample collected from the subject; an information acquisition step of acquiring information about the risk of developing exfoliation syndrome or exfoliation glaucoma in the subject on the basis of the results of the measurement of the alleles; and an information provision step of providing information for determining the risk of developing exfoliation syndrome or exfoliation glaucoma in the subject on the basis of the information acquired in the preceding step. According to the method of the present invention, it becomes possible to determine the presence or absence of the risk of developing exfoliation syndrome or exfoliation glaucoma in a subject and predict the degree of the aforementioned risk in the subject, by analyzing SNPs of the present invention occurring in a sample from the subject.
机译:一种辅助诊断受试者中剥脱综合征或剥脱性青光眼的风险的方法,所述方法包括:等位基因测量步骤,测量等位基因的至少30个单核苷酸多态性(SNP),包括表1中所列的12个核心SNP。基于从受试者收集的生物样品中的SNP等位基因信息,从表2中列出的合并SNP中选择的SNP(选定的合并SNP);信息获取步骤,基于等位基因的测量结果,获取与受试者发生剥脱综合症或剥脱性青光眼的风险有关的信息;信息提供步骤,其基于在先前步骤中获取的信息,提供用于确定对象中发生剥脱综合症或剥脱性青光眼的风险的信息。根据本发明的方法,通过分析本发明的SNP,可以确定受试者中是否存在剥脱综合征或剥脱性青光眼的风险,并预测受试者中上述风险的程度。发生在受试者的样本中。

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