Laboratory of Cytogenetics, Pasteur Institute of Morocco, Casablanca, Morocco.
Laboratory of Physiopathology and Molecular Genetics, Faculty of Sciences Ben M'Sik, Hassan II University, Casablanca, Morocco.
Biomed Res Int. 2021 May 5;2021:8893467. doi: 10.1155/2021/8893467. eCollection 2021.
Chromosomal abnormalities are the main genetic risk factor associated with reproductive and sexual development disorders (DSD). The goal of this study is to retrospectively evaluate the frequency of chromosomal aberrations in Moroccan subjects with problems of procreation or sexual ambiguity. A total of 1005 individuals, including 170 infertile couples, underwent cytogenetic analysis in the Cytogenetic Laboratory of the Pasteur Institute of Morocco. Heparinized blood samples were processed according to the standard karyotype method. A total (81.5%) of the patients studied had a normal karyotype, while the remaining (18.5%) patients had an abnormal karyotype. Female patients had more chromosomal abnormalities (52%) than male patients (48%). These chromosomal aberrations included 154 cases (83%) of sex chromosomal abnormalities, the most common being Turner's syndrome and Klinefelter's syndrome, and 31 cases (17%) had autosomal aberrations, especially chromosome 9 reversal (inv(9)(p12;q13)). The present data shows that among 170 couples, 10.6% had chromosomal abnormalities mainly involved in the occurrence of recurrent miscarriages. Genotype-phenotype correlations could not be made, and therefore, studies using more resolutive molecular biology techniques would be desirable.
染色体异常是与生殖和性发育障碍(DSD)相关的主要遗传风险因素。本研究的目的是回顾性评估有生育问题或性发育模糊的摩洛哥患者的染色体异常频率。共有 1005 名个体,包括 170 对不育夫妇,在摩洛哥巴斯德研究所的细胞遗传实验室进行了细胞遗传学分析。肝素化的血液样本按照标准核型方法进行处理。研究中总共有(81.5%)的患者具有正常核型,而其余(18.5%)患者具有异常核型。女性患者的染色体异常(52%)比男性患者(48%)更多。这些染色体异常包括 154 例(83%)性染色体异常,最常见的是特纳综合征和克莱恩费尔特综合征,31 例(17%)有常染色体异常,特别是 9 号染色体倒位(inv(9)(p12;q13))。目前的数据表明,在 170 对夫妇中,有 10.6%的夫妇存在染色体异常,主要涉及反复流产的发生。无法进行基因型-表型相关性分析,因此,需要使用更具分辨率的分子生物学技术进行研究。