Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.

Annales de genetique Pub Date : 1999-01-01
C H Wouters, T M van Bodegom, H A Moll, L C Govaerts
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引用次数: 0

Abstract

A male infant with a deletion of 9p and concomitant duplication of 4q: 46,XY, der(9)t(4;9)(q27;p24), is described. Parental chromosome analysis showed a balanced maternal translocation. To our knowledge, the above cytogenetic and clinical abnormalities have not been described previously. A phenotype comparison is presented with previously reported cases concerning a deletion of 9p and a duplication of 4q.

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由家族易位t(4;9)(q27;p24)引起的儿童后肛门闭锁的4q部分三体和9p单体。
描述了一名男婴9p缺失并伴随4q: 46,XY, der(9)t(4;9)(q27;p24)的重复。亲本染色体分析显示一个平衡的母体易位。据我们所知,上述细胞遗传学和临床异常以前没有描述过。表型比较与先前报道的病例有关9p的缺失和4q的重复提出。
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