患有46,XY疾病或性别发育差异的患者的DHX37变异
Yuko Katoh-Fukui1, Daisuke Saito2, Hiroko Narumi2,3
1Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan. fukui-y@ncchd.go.jp.
Human genome variation
|September 7, 2025
概括
对患有46,XY性发育障碍的日本患者的基因分析揭示了DEAH-box酶37 (DHX37) 中的致病变体. 这突显了与DHX37变体相关的遗传和表型多样性.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 内分泌学 在内分泌学.
背景情况:
- 46,XY性发育障碍 (DSD) 代表了一组异质的疾病.
- 遗传因素在DSD的病因学中起着至关重要的作用.
- 了解DSD的遗传基础对于诊断和管理至关重要.
研究的目的:
- 在日本队列中调查DSD的遗传景观.
- 为了识别与46,XY DSD相关的新型遗传变异.
- 描述与已识别的变异相关的表型谱,特别是在DHX37.
主要方法:
- 在17名具有46,XY DSD.的日本患者身上进行了全外组测序.
- 进行了变异调用和致病性评估.
- 临床表型与已识别的遗传变异相关.
主要成果:
- 在3名患者中发现了DEAH-box酶37 (DHX37) 的两种致病变体.
- 在一名患者中发现了SOX9的可能致病变体.
- 在DHX37中还发现了一种罕见的,可能是良性变异.
结论:
- 这项研究在46,XY DSD.患者中确定了致病性DHX37变体.
- 这些发现强调了与DHX37.7相关的遗传和表型多样性.
- DHX37与46,XY DSD的病因有关,有助于更广泛地了解性发育障碍.
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