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香港原发性和继发性闭经患者的细胞遗传学分析:回顾性研究。

Cytogenetic analysis of patients with primary and secondary amenorrhoea in Hong Kong: retrospective study.

作者信息

Wong M S F, Lam S T S

机构信息

Department of Obstetrics and Gynaecology, Kwong Wah Hospital, 25 Waterloo Road, Hong Kong.

出版信息

Hong Kong Med J. 2005 Aug;11(4):267-72.

Abstract

OBJECTIVE

To estimate the incidence and type of chromosomal abnormalities in patients with primary and secondary amenorrhoea in Hong Kong.

DESIGN

Cytogenetic analysis and retrospective review.

SETTING

Clinical Genetic Service, Department of Health, Hong Kong.

PATIENTS

Case records of 549 patients with either primary (n=237) or secondary (n=312) amenorrhoea referred to the Clinical Genetic Service from 1 January 1991 to 30 April 2002 were reviewed. All these patients with amenorrhoea would have karyotyping (G banding) performed.

MAIN OUTCOME MEASURES

Clinical characteristics of patients, and incidence and type of chromosomal abnormalities in the local population.

RESULTS

Sex chromosome anomaly was found in 24.5% and 9.9%, respectively, of women with primary and secondary amenorrhoea. In those with primary amenorrhoea, male karyotype was identified in 8.4% and X-chromosome abnormalities in 16.0%.

CONCLUSION

The incidence of chromosomal abnormalities in women with amenorrhoea is similar to that reported in the literature. Chromosomal abnormalities are identified often enough to warrant karyotyping of all women with amenorrhoea.

摘要

目的

评估香港原发性和继发性闭经患者染色体异常的发生率及类型。

设计

细胞遗传学分析及回顾性研究。

地点

香港卫生署临床遗传服务部。

患者

回顾了1991年1月1日至2002年4月30日转诊至临床遗传服务部的549例原发性闭经(n = 237)或继发性闭经(n = 312)患者的病例记录。所有这些闭经患者均进行了核型分析(G显带)。

主要观察指标

患者的临床特征,以及当地人群染色体异常的发生率及类型。

结果

原发性闭经和继发性闭经女性中,性染色体异常的发生率分别为24.5%和9.9%。在原发性闭经患者中,8.4%为男性核型,16.0%为X染色体异常。

结论

闭经女性染色体异常的发生率与文献报道相似。染色体异常的检出率足以证明应对所有闭经女性进行核型分析。

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