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通过染色体分析诊断基因缺陷。

Diagnosis of genetic defects by chromosomal analysis.

作者信息

Ghani F, Maniar S, Khilji Z, Azim M, Khurshid M

机构信息

Department of Pathology, Aga Khan University Hospital, Karachi.

出版信息

J Pak Med Assoc. 1995 Nov;45(11):295-6.

PMID:8920609
Abstract

Of 901 karyotypes performed over a period of 4 years, genetic anomalies were detected in 162 cases. Down's syndrome (trisomy 21) was the most common (168.8%) genetic disorder followed by Turner's syndrome, Philadelphia chromosome, Klinefelter's syndrome, Edward's syndrome (trisomy 18) and Patau's syndrome (trisomy 13). All the three trisomies were detected very early in life. Mean age at the time of diagnosis for Turner's syndrome was 13.3 years, allowing a timely hormone replacement therapy to improve secondary sexual characters. Patients with Klinefelter's syndrome were diagnosed late (mean age 23.6 years), which greatly reduced their chances of an effective therapy to improve the clinical and social outcome.

摘要

在4年期间进行的901例核型分析中,在162例中检测到基因异常。唐氏综合征(21三体)是最常见的(168.8%)基因疾病,其次是特纳综合征、费城染色体、克氏综合征、爱德华兹综合征(18三体)和帕陶氏综合征(13三体)。所有这三种三体综合征在生命早期就被检测到。特纳综合征诊断时的平均年龄为13.3岁,这使得能够及时进行激素替代疗法以改善第二性征。克氏综合征患者诊断较晚(平均年龄23.6岁),这大大降低了他们获得有效治疗以改善临床和社会结局的机会。

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