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家族性无脑儿中存在主基因的证据。

Evidence for a major gene in familial anencephaly.

作者信息

Shaffer L G, Marazita M L, Bodurtha J, Newlin A, Nance W E

机构信息

Department of Human Genetics, Medical College of Virginia, Richmond.

出版信息

Am J Med Genet. 1990 May;36(1):97-101. doi: 10.1002/ajmg.1320360119.

Abstract

A 21-year-old white woman sought counseling after the birth of two consecutive anencephalic male fetuses with complete rachischisis and discordant renal dysplasia. The presence of parental consanguinity prompted reconsideration of recessive inheritance. The segregation ratio from 23 additional consanguineous cases was compared with that observed in 294 presumably nonconsanguineous families previously reported. Using classical segregation analysis, the segregation ratios in the non-sporadic cases were consistent with a major autosomal recessive locus in both populations.

摘要

一名21岁的白人女性在连续两次产下无脑男胎后寻求咨询,这两个胎儿均患有完全脊柱裂和不一致的肾发育异常。父母近亲结婚的情况促使人们重新考虑隐性遗传。将另外23例近亲结婚病例的分离比与之前报道的294个可能非近亲结婚家庭中观察到的分离比进行了比较。使用经典分离分析,在两个群体中,非散发病例的分离比均与一个主要常染色体隐性基因座一致。

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