Badner J A, Chakravarti A
Division of Human Genetics, Graduate School of Public Health, University of Pittsburgh.
Am J Med Genet. 1990 Jan;35(1):100-4. doi: 10.1002/ajmg.1320350119.
Segregation and linkage analysis was performed on published data on 5 families segregating for Waardenburg syndrome (WS) and Hirschsprung disease (HRSD). Two of these families demonstrated parental consanguinity. On the basis of these families, autosomal recessive inheritance of the combination WS-HRSD has been postulated. However, a single dominant gene with pleiotropic effects leading to WS and HRSD, with a more severe phenotype in homozygotes, is more plausible. A model of gene action incorporating stochastic effects is compatible with these observations.
对已发表的5个家系的数据进行了分离分析和连锁分析,这些家系中Waardenburg综合征(WS)和先天性巨结肠病(HRSD)呈分离状态。其中两个家系显示出父母近亲结婚。基于这些家系,推测WS-HRSD组合为常染色体隐性遗传。然而,一个具有多效性作用的单一显性基因导致WS和HRSD,且纯合子中表型更严重,这种情况似乎更合理。一个纳入随机效应的基因作用模型与这些观察结果相符。