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DAX1基因突变所致先天性肾上腺皮质发育不全伴低促性腺激素性腺发育不全三例 被引量:1

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摘要 DAX1基因突变所致的先天性X连锁肾上腺皮质发育不全(adrenal hypoplasia congenita,AHC)伴低促性腺激素性腺发育不全(hypogonadotrophic hypogonadism,HH)全球报道不过百余例。我院于2007年首次确诊国内表兄弟2人同患该病,以后又确诊了3例病患。由于该病诊断困难,更无相应诊疗常规,故将这3例患者的诊治经验报道如下。
出处 《中华医学杂志》 CAS CSCD 北大核心 2010年第30期2159-2160,共2页 National Medical Journal of China
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  • 1杨军,张惠杰,肖园,王伟,王卫庆,李小英,宁光.DAX-1基因缺陷所致两例先天性肾上腺发育不良症[J].中华内分泌代谢杂志,2007,23(5):475-477. 被引量:11
  • 2Weiss L,Mellinger R C.Congenital adrenal hypoplasia--an X-linked disease.J Med Genet,1970,7:27-32.
  • 3Muscatelli F,Strom T M,Walker A P,et al.Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.Nature,1994,372:672-676.

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  • 7Goto M, Katsumata N. X-linked adrenal hypoplasia congenita caused by a novel intronic mutation of the DAX-I gene[J]. Horm Res,2009,71(2) : 120-124.
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  • 10张化冰,聂敏.先天性肾上腺发育不良伴低促性腺激素性性腺功能不全患者的临床及分子遗传学研究[J].生殖医学杂志,2011,20(3):183-187. 被引量:5

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