由父亲遗传易位(4:18)导致的4号部分三体(q26 - qterminal)儿童与多种先天性异常和死亡相关

Q4 Biochemistry, Genetics and Molecular Biology
Genome Integrity Pub Date : 2019-05-24 eCollection Date: 2019-01-01 DOI:10.4103/genint.genint_4_18
Abhik Chakraborty, Santosh Kumar Panda, Nirmal Kumar Mohakud, Debarshi Roy, Swatishree Padhi, Shu Wen Koh, Manoor Prakash Hande, Birendranath Banerjee
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引用次数: 1

摘要

在配子发生过程中,由于减数分裂分离不平衡,亲本平衡的互惠易位可导致后代部分非整倍性。在这里,我们报告了一个9天大的4号染色体部分三体的男孩的表型和细胞遗传学特征。先证者和父母的染色体核型与父本染色体的多色荧光原位杂交(mFISH)一起进行。先证者核型为47、XY、der(18)、t(4;18)(q26;q22)、+4,父本核型为47、XY、der(18)、t(4;18)(q26;q22)。对父亲染色体准备的mFISH分析证实了平衡易位的区域和起源。在这项研究中,核型分析帮助我们确定了先证者的数量和结构异常,mFISH帮助我们确认了我们的细胞遗传学发现。因此,建议在怀孕前对双方进行细胞遗传学筛查,以排除或确认任何一方、双方或任何一方的数字或结构异常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Child with Partial Trisomy 4 (q26 - qterminal) Resulting from Paternally Inherited Translocation (4:18) Associated with Multiple Congenital Anomalies and Death.

A Child with Partial Trisomy 4 (q26 - qterminal) Resulting from Paternally Inherited Translocation (4:18) Associated with Multiple Congenital Anomalies and Death.

A Child with Partial Trisomy 4 (q26 - qterminal) Resulting from Paternally Inherited Translocation (4:18) Associated with Multiple Congenital Anomalies and Death.

A Child with Partial Trisomy 4 (q26 - qterminal) Resulting from Paternally Inherited Translocation (4:18) Associated with Multiple Congenital Anomalies and Death.

Parental balanced reciprocal translocations can result in partial aneuploidy in the offspring due to unbalanced meiotic segregation during gametogenesis. Herein, we report the phenotypic and cytogenetic characterization in a 9-day-old male child with partial trisomy of chromosome 4. Karyotyping of the proband and parents was performed along with multicolor fluorescence in situ hybridization (mFISH) of paternal chromosomes. Conventional cytogenetic analysis by karyotyping showed 47,XY,der(18),t(4;18)(q26;q22),+4 in proband, and the paternal karyotype was found as 47,XY,der(18),t(4;18)(q26;q22). mFISH analysis on paternal chromosomal preparations confirmed both region and origin of the balanced translocation. In this study, karyotyping helped us to identify both numerical and structural anomalies in the proband, and mFISH helped us to confirm our cytogenetic findings. Therefore, cytogenetic screening of both partners is recommended before pregnancy to rule out or confirm the presence of any numerical or structural anomaly in one, both, or none of the partners.

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来源期刊
Genome Integrity
Genome Integrity Biochemistry, Genetics and Molecular Biology-Genetics
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