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A Study on Chromosomal Analysis of Patients with Primary Amenorrhea

机译:原发性闭经患者的染色体分析研究

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Background: Primary amenorrhea is one of the most common disorders seen as gynecological problems in adolescent girls. It refers to the participants who did not attain menarche by the age of 11–15 years. Chromosome abnormalities contribute as one of the etiological factors in patients with primary amenorrhea. Aims: The aim of this study was to evaluate the frequency of chromosomal abnormalities and to investigate the abnormal karyotypes in patients referred with the symptom of primary amenorrhea for better management and counseling. Setting and Design: One hundred and seventy-four cases of primary amenorrhea were referred from the obstetrics and gynecology department to our cytogenetic laboratory for chromosomal analysis. G-banded chromosomes were karyotyped, and chromosomal analysis of all patients was done. Results: Out of 174 patients, we observed 23 (13.22%) participants with abnormal karyotype. In 23 cases of chromosomal abnormalities, 10 cases were sex reversal female (46,XY) and Turner karyotype (45,X) in 6 females. Other numerical and structural abnormalities were also seen such as 47,XXX; 45,X/47,XXX; 45,X/46, X,dic(X); 46,XX, inv (9); 45,X/46,X,i(Xq); 46,X,mar(X); and 45,X/46,XY in the primary amenorrhea cases. Conclusion: This study definitely attests the importance of chromosomal analysis in the etiologic diagnosis of primary amenorrhea patients. Karyotyping will help to counsel and manage the cases of primary amenorrhea in a better way. This study reveals the frequencies and different types of chromosomal abnormalities found in primary amenorrhea individuals and that might help to make the national database on primary amenorrhea in relation to chromosomal aberrations.
机译:背景:原发性闭经是青春期最常见的疾病之一,被视为女性的妇科问题。它指的是到11-15岁尚未初潮的参与者。染色体异常是原发性闭经患者的病因之一。目的:本研究的目的是评估患有原发性闭经症状的患者的染色体异常频率并调查其异常核型,以便进行更好的管理和咨询。设置与设计:174例原发性闭经从妇产科转到我们的细胞遗传学实验室进行染色体分析。对G带染色体进行了染色体核型分析,并对所有患者进行了染色体分析。结果:在174例患者中,我们观察到23名(13.22%)核型异常的参与者。在23例染色体异常病例中,有6例女性中有10例为性逆转女性(46,XY)和Turner核型(45,X)。还发现了其他数字和结构异常,例如47,XXX。 45,X / 47,XXX; 45,X / 46,X,dic(X); 46,XX,inv(9); 45,X / 46,X,i(Xq); 46,X,mar(X);在原发性闭经病例中为45,X / 46,XY。结论:这项研究肯定证明了染色体分析在原发性闭经患者病因诊断中的重要性。核型分析将有助于更好地指导和管理原发性闭经的病例。这项研究揭示了在原发性闭经个体中发现的染色体异常的频率和不同类型,这可能有助于建立与染色体畸变有关的原发性闭经的国家数据库。

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