The 47,XXY karyotype and unrelated malformative patterns: an unusual association.

Helvetica paediatrica acta Pub Date : 1987-06-01
M Aricò, A Colombo, E Maserati, F Pasquali, G R Burgio
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Abstract

47,XXY chromosome complement is relatively frequent (1/750-1000 male newborns) but has so far not been reported in association with malformative syndromes. Three cases of 47,XXY karyotype associated with an unrelated malformative pattern, the Silver-Russell syndrome in two cases and Noonan syndrome in one case are reported. The possibility of a phenotypic alteration of patients with the XXY karyotype by these malformative syndromes is considered.

47,xxy核型和不相关的畸形模式:一种不寻常的关联。
XXY染色体补体比较常见(1/750-1000男性新生儿),但迄今尚未报道与畸形综合征有关。本文报告了3例47,xxy核型与不相关的畸形模式相关的病例,其中银罗素综合征2例,努南综合征1例。考虑到这些畸形综合征对XXY核型患者的表型改变的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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