...健否网 2009年4月26日 [ 健否网] [ 推荐给朋友] [ 健否问答] [ 收藏] 先天性肾腺皮质增生症(Congenital adrenal hyperplasia,CAH).是种较常见常染色体隐性遗传病,由于肾腺皮质激素合成过程中所需酶先天性缺陷所致.
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婴儿骨皮质增生症 Caffey disease ; infantile cortical hyperostosis ; ICH
肾上腺皮质增生症 congenital adrenal cortical hyperplasia ; CAH
婴儿性骨皮质增生症 infantile cortical hyperostosis
骨皮质增生症 infantile cortical hyperostosis ; ICH
天性肾上腺皮质增生症 congenital adrenal cortical hyperplasia ; congenital adrenal hyperplasia
婴儿型号骨皮质增生症 infantile cortical hyperostosis ; ICH
性肾上腺皮质增生症 CLAH ; congenital adrenal hyperplasia
腺皮质增生症 Congenital adrenal hyperplasia ; CAH
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.
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