一个DAX1缺乏的家庭中的四个成员之间的表型变异
Yuko Seki1, Haruna Kakimoto1, Izumi Tamada2
1Department of Pediatrics, 208512 Kagoshima University Graduate School of Medical and Dental Science , Kagoshima, Japan.
Journal of pediatric endocrinology & metabolism : JPEM
|July 27, 2025
概括
由新型NR0B1变体引起的DAX1缺乏症,在四个家庭成员中表现出不同的症状和发病年龄. 对于有这种疾病家族史的男性,建议进行遗传确认.
科学领域:
- 遗传学 是一个遗传学.
- 内分泌学 在内分泌学.
- 儿科 儿科 儿科
背景情况:
- DAX1 (剂量敏感性性别逆转-上腺生性缺血X染色体基因1的临界区域) 缺陷是一种罕见的遗传性疾病.
- NR0B1基因的突变是DAX1缺乏的主要原因,导致上腺功能不充分.
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