摘要
先天性智力低下及畸形是进行染色体检查的适应症。本文对34例智力低下和畸形的患儿做了染色体核型分析。发现染色体异常者为10例,占受检者的29.4%。21三体占异常染色体的60%,其他还有22三体,47XYY以及嵌合型等等,为临床的诊断和治疗提供了准确依据。
Patients who suffer from the congenital low intelletual faculties and deformity should be inspeeted with chromoeoms karyotype analysis. 34 cases with above-mentioned clinical symptoms were made into chromosome karyotype analysis. Of them, 10 cases were found with abnormal chromosome karyothpe which make up 29.4%. Among abnormal chromioml karyotype there were 21 triploid(60%), 22 triploid, 47,XYY and its mosaic, and others. All these would supply an exact clinical diagnosis.
出处
《锦州医学院学报》
1999年第3期14-15,共2页
Journal of Jinzhou Medical College