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34例智力低下及畸形儿的染色体核型分析

THE CHROMOSOME KARYOTYPE ANALYSIS OF 34 CASES WITH LOW INTELLECTUAL FACULTIES AND DEFORMITY
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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
关键词 智力低下 染色体核型 畸形儿 儿童 chromosome karyotype low intellectual faculties
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  • 1杨爱德.染色体畸变与临床[J]实用儿科杂志,1988(04).

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