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由于家族性t(6;13)(p22;q34或33)易位,6号染色体短臂2区2带三体导致6号染色体短臂末端。

Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.

作者信息

Rosi G, Venti G, Migliorini Brushelli G, Donti E, Bocchini V, Armellini R

出版信息

Hum Genet. 1979 Sep 2;51(1):67-72. doi: 10.1007/BF00278294.

Abstract

A newborn with a 46,XY,der(13),t(6;13)(p22;q34 or 33)pat karyotype, trisomic for the 6p22 leads to 6pter segment and, perhaps, monosomic for the 13q telomere, is reported. The balanced translocation is familial and was also encountered in the sister and paternal grandmother. The infant's phenotype was similar to that described in seven previously reported cases of partial trisomy 6p and further supports a partial trisomy 6p syndrome as proposed by Breuning et al.

摘要

报告了一名核型为46,XY,der(13),t(6;13)(p22;q34或33)pat的新生儿,其6p22三体导致6pter片段,可能13q端粒单体。这种平衡易位是家族性的,在其姐姐和祖母中也有发现。该婴儿的表型与之前报道的7例部分6p三体病例相似,进一步支持了Breuning等人提出的部分6p三体综合征。

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