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先天性肾上腺皮质增生症(congenital adrenal hyperplasia, CAH)是一组由基因突变导致肾上腺皮质激素合成障碍的常染色体隐性遗传病。CAH育龄期女性患者妊娠率及活产率明显下降。本文报道1例失盐型CAH患者经过内分泌科和生殖中心共同治疗,最终行体外受精-胚胎移植后成功妊娠的诊疗过程。
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基本信息:
中图分类号:R586;R714.8
引用信息:
[1]范融,王含必,邓成艳,等.失盐型21羟化酶缺乏症行体外受精-胚胎移植1例分析及文献复习[J].生殖医学杂志,2021,30(09):1244-1246.
2021-09-15
2021-09-15