为了测试性激素造成的影响，研究人员选取的对象是患有先天肾上腺增生症（congenital adrenal hyperplasia ，CAH)的男女青年以及刚成年的人。因为遗传原因，相比那些健康的孩子，出生前他们接触到的雄性激素更多。
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羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。
DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
目的开展新生儿先天性肾上腺皮质增生症筛查，降低残疾儿童的发生率，提高人口素质。
Objective to develop the neonatal screening for congenital adrenal hyperplasia in order to prevent children from congenital disability and improve the aristogenesis in our country.
结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
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