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克莱因费尔特综合征中的矮身来自Aggrecan突变
Antoinette Farrell1, Sunitha R Sura1,2
1Department of Pediatrics, University of Connecticut School of Medicine, Hartford, CT 06106, USA.
JCEM case reports
|October 4, 2024
概括
克莱因费尔特综合征 (KS) 中的矮身可能源于遗传变异. 一名16岁的KS患者因新型ACAN基因变异而身高矮,突出了对受影响个体进行基因测试的需要.
科学领域:
- 遗传学 遗传学 是一个
- 内分泌学 在内分泌学.
- 儿科 儿科 儿科
背景情况:
- 克莱因费尔特综合征 (KS) 通常表现为高个体.
- 在KS中,矮身通常与生长激素 (GH) 缺乏有关.
- 除了GH缺乏之外的遗传因素也可能导致KS患者的矮身.
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