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利用肌酸激酶测定和DNA分析对贝克肌营养不良症进行携带者检测。

Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.

作者信息

Kingston H M, Sarfarazi M, Newcombe R G, Willis N, Harper P S

出版信息

Clin Genet. 1985 Apr;27(4):383-91. doi: 10.1111/j.1399-0004.1985.tb02280.x.

Abstract

Serum creatine kinase levels in 39 control females and 59 obligate carriers of Becker muscular dystrophy (BMD) have been used to construct likelihood ratios for carrier detection. In 24 possible carriers of BMD, analysis of DNA with X chromosome specific DNA probes linked to the dystrophy gene, has been used in conjunction with creatine kinase measurement to calculate final risk estimates of carrier status. Incorporation of information from probe genotype into the Bayesian calculation, enables a substantially lower risk to be deliniated for some possible carriers of the BMD gene. Thus, although the existing DNA probes are not sufficiently closely linked to BMD to be used in prenatal diagnosis, they can make a major contribution to genetic counseling by refining the estimated probability of carrier status.

摘要

39名对照女性和59名贝克型肌营养不良症(BMD)的 obligate携带者的血清肌酸激酶水平已被用于构建携带者检测的似然比。在24名可能的BMD携带者中,使用与肌营养不良症基因相连的X染色体特异性DNA探针进行DNA分析,并结合肌酸激酶测量来计算携带者状态的最终风险估计值。将探针基因型信息纳入贝叶斯计算,能够为一些可能的BMD基因携带者划定显著更低的风险。因此,尽管现有的DNA探针与BMD的连锁不够紧密,无法用于产前诊断,但它们可以通过细化携带者状态的估计概率,对遗传咨询做出重大贡献。

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