2011Journal of Practical Obstetrics and GynecologyRequires access

Clinical Analysis of 184 Cases with Chromosomal Abnormality in 1624 Infertility Patients

Ren Meihong

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Abstract

Objective:To study the relationship between chromosome abnormity and their phenotype, and analyze the detection rate of abnormal chromosome, abnormal phenotype and frequency distribution.Methods:Among 1624 patients consulted in infertility clinic in our hospital from recent 6 years, chromosome karyotype and clinical analysis were conducted in abnormal chromosome patients.Results:Out of 1624 infertility patients, 184 cases were with chromosome abnormity. The numbers of euchromosome abnormalities were 79 (42.93%). The number of sex chromosome abnormalities and abnormal sex chromosome structure were 31 and 74, respectively, and they accounted for 16.85% and 40.22%, respectively. Among 184 cases with abnormal chromosome, 21 cases were azoospermia (11.41%) and 23 cases were oligospermia (12.50%). 96 cases were recurrent spontaneous abortion and multiple fetal death during pregnancy (52.17%). Delivery of terata was 23 (12.50%), mental retardation and abnormal development were 21 (11.41%).Conclusions:Chromosome abnormity is one of the important factors in patients with infertility. Chromosome examination should be performed to exclude the possibility of chromosome abnormity in patients with obstinate infertility.

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Objective:To study the relationship between chromosome abnormity and their phenotype, and analyze the detection rate of abnormal chromosome, abnormal phenotype and frequency distribution.Methods:Among 1624 patients consulted in infertility clinic in our hospital from recent 6 years, chromosome karyotype and clinical analysis were conducted in abnormal chromosome patients.Results:Out of 1624 infertility patients, 184 cases were with chromosome abnormity. The numbers of euchromosome abnormalities were 79 (42.93%). The number of sex chromosome abnormalities and abnormal sex chromosome structure were 31 and 74, respectively, and they accounted for 16.85% and 40.22%, respectively. Among 184 cases with abnormal chromosome, 21 cases were azoospermia (11.41%) and 23 cases were oligospermia (12.50%). 96 cases were recurrent spontaneous abortion and multiple fetal death during pregnancy (52.17%). Delivery of terata was 23 (12.50%), mental retardation and abnormal development were 21 (11.41%).Conclusions:Chromosome abnormity is one of the important factors in patients with infertility. Chromosome examination should be performed to exclude the possibility of chromosome abnormity in patients with obstinate infertility.

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Available abstract

Objective:To study the relationship between chromosome abnormity and their phenotype, and analyze the detection rate of abnormal chromosome, abnormal phenotype and frequency distribution.Methods:Among 1624 patients consulted in infertility clinic in our hospital from recent 6 years, chromosome karyotype and clinical analysis were conducted in abnormal chromosome patients.Results:Out of 1624 infertility patients, 184 cases were with chromosome abnormity. The numbers of euchromosome abnormalities were 79 (42.93%). The number of sex chromosome abnormalities and abnormal sex chromosome structure were 31 and 74, respectively, and they accounted for 16.85% and 40.22%, respectively. Among 184 cases with abnormal chromosome, 21 cases were azoospermia (11.41%) and 23 cases were oligospermia (12.50%). 96 cases were recurrent spontaneous abortion and multiple fetal death during pregnancy (52.17%). Delivery of terata was 23 (12.50%), mental retardation and abnormal development were 21 (11.41%).Conclusions:Chromosome abnormity is one of the important factors in patients with infertility. Chromosome examination should be performed to exclude the possibility of chromosome abnormity in patients with obstinate infertility.

Key concepts: Infertility, Azoospermia, Medicine, Karyotype, Chromosome, Abnormality, Chromosome abnormality, Oligospermia

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