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[通过苯丙氨酸口服负荷检测苯丙酮尿症杂合子]

[Heterozygote detection in phenylketonuria by means of an oral load of phenylalanine].

作者信息

Dhondt J L, Farriaux J P

出版信息

J Genet Hum. 1979 Jun;27(2):145-56.

PMID:396362
Abstract

The testing of heterozygosity for PKU by mean of an oral load of phenylalanine is a widely used method. In this paper, the need of a genetic counselling for two adults, with family story of PKU, lead us to reinvestigate criteria of heterozygote recognition. With all variables of the phenylalanine tolerance test, overlapping and mis classification occured. Probability density functions plotting, as proposed by GOLD, illustrated well the genetic risk of a patient. However, in practice, the heterozygote likelihood ratio determination seemed to be the best way to avoid possibly erroneous categoric statement by correcting the ratio for the a priori probability of heterozygosity.

摘要

通过口服苯丙氨酸负荷来检测苯丙酮尿症(PKU)杂合性是一种广泛使用的方法。在本文中,两名有PKU家族病史的成年人需要进行遗传咨询,这促使我们重新研究杂合子识别标准。在苯丙氨酸耐量试验的所有变量中,出现了重叠和错误分类的情况。正如戈尔德所提出的,概率密度函数绘图很好地说明了患者的遗传风险。然而,在实践中,杂合子似然比的测定似乎是避免因校正杂合性先验概率的比率而可能产生错误分类陈述的最佳方法。

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3
Heterozygote detection in phenylketonuria.苯丙酮尿症杂合子检测
Clin Genet. 1977 Feb;11(2):137-46. doi: 10.1111/j.1399-0004.1977.tb01291.x.

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