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.
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.
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.
方法总结15例肾上腺性征综合征患者的临床资料，其中先天性肾上腺皮质增生13例，肾上腺皮质癌2例。
Methods The clinical data of 15 patients were summarized including 13 cases of congenital adrenal hyperplasia, and 2 cases of adrenocortical carcinoma.
方法总结15例肾上腺性征综合征患者的临床资料，其中先天性肾上腺皮质增生13例，肾上腺皮质癌2例。
Methods The clinical data of 15 patients were summarized including 13 cases of congenital adrenal hyperplasia, and 2 cases of adrenocortical carcinoma.
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