DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenitaladrenalhyperplasia with 21-hydroxylase deficiency.
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。
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Methods The clinical data of 15 patients were summarized including 13 cases of congenitaladrenalhyperplasia, 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。
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Objective to develop the neonatal screening for congenitaladrenalhyperplasia in order to prevent children from congenital disability and improve the aristogenesis in our country.