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Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.

机译:胎儿表型在21三分体和22分体中发现。

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摘要

Prenatal diagnosis was performed in a woman whose previous pregnancy resulted in a girl with probable Down syndrome who died soon after delivery. The mother was found to be a carrier of a reciprocal balanced translocation between chromosomes 21 and 22, and the fetus was found to have an unbalanced translocation involving chromosomes 21 and 22: 46,XX, -22, +t(21;22)(q22;q11)(21 pter leads to 21q22::22q11 leads to 22qter). Despite partial monosomy for the proximal segment of 22 and trisomy for proximal 21, the fetus did not have gross external abnormalities, but several internal malformations were found. To our knowledge, this is the first time that this unbalanced karyotype has been described.
机译:对一名妇女进行了产前诊断,该妇女的先前妊娠导致一名可能患有唐氏综合症的女孩在分娩后不久死亡。发现母亲是21号和22号染色体之间相互平衡易位的载体,而发现胎儿具有21号和22号染色体的不平衡易位:46,XX,-22,+ t(21; 22)( q22; q11)(21 pter导致21q22 :: 22q11导致22qter)。尽管22的近端部分进行部分单体切割,而21的近端进行了三体切割,但胎儿并没有明显的外部异常,但是发现了一些内部畸形。据我们所知,这是第一次描述这种不平衡核型。

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