在WNT10B底层非综合征分裂手/脚形中存在序列变异
Muhammad Bilal1,2,3, Tobias B Haack3, Rebecca Buchert3
1Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
Molecular syndromology
|December 7, 2023
概括
在WNT10B基因的遗传变异导致分裂手脚形 (SHFM),一个罕见的肢体缺陷. 这项研究确定了一种新的WNT10B变种,在两个家族中导致SHFM.
科学领域:
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
- 医学遗传学 医学遗传学
背景情况:
- 分手和足部形 (SHFM),也称为外肢形,是一种罕见的四肢形.
- 由于中枢光线发育受损或不存在,SHFM的特征是手和脚的中间裂.
- 它可以表现为一个孤立的条件或与其他发育异常一起.
研究的目的:
- 在两个家庭中确定非综合征性SHFM的遗传原因.
- 研究WNT10B基因变异在肢体发育障碍中的作用.
主要方法:
- 两个非综合征性SHFM家族的临床表型.
- 整体外基因组测序和桑格测序以检测引起的遗传变异.
主要成果:
- 在两个家族的受影响个体中,WNT10B基因中发现了两种致病变异.
- 在A.家族中发现了一种新的误解变体 (c.338G>C; p.(Gly113Ala)).
- 在B.家族中发现了一种以前报告的移变异 (c.884-896delTCCAGCCCCCCGTCT; p.(Phe295Cysfs*87)).
结论:
- 这项研究确定了一种新的WNT10B变体是SHFM的原因.
- 这些发现扩大了对SHFM和肢体发育的遗传基础的理解.
- 结果提供了对肢体形背后的分子机制的见解.
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