一个X结合的低水分性外皮形患者的小牙类表型,该患者患有新型EVC2变异
Yi Wu1, Jing Sun1, Caiqi Zhang1
1The Stomatology Center of Xiangya Hospital, Academician Workstation for Oral & Maxillofacial Regenerative Medicine, Research Center of Oral and Maxillofacial Development and Regeneration, National Clinical Research Center for Geriatric Diseases, Central South Universtiy, Changsha, Hunan Province, China.
Heliyon
|January 1, 2024
概括
这项研究确定了低水分性外皮性形症 (HED) 的新型基因变异,揭示了EDA和EVC2变异对寡头症严重性的潜在协同效应.
科学领域:
- 遗传学 是一个遗传学.
- 发展生物学 发展生物学
- 口腔健康 口腔健康
背景情况:
- 缺水性外皮性形症 (HED) 是一种影响外皮结构的遗传性疾病.
- 寡牙,HED的一个关键特征,涉及先天缺少多个牙.
研究的目的:
- 在患有HED和寡牙的患者中调查致病基因.
- 探索已识别的基因变异与寡类现象型的严重程度之间的关系.
主要方法:
- 在患者的DNA上进行了全外体序列 (WES) 测序.
- 使用桑格测序证实了已识别的变异.
- 在分析预测了蛋白质变异的功能影响.
主要成果:
- 一种半体EDA变种 (c.466C>T p.(Arg156Cys)) 和一种新型异体EVC2变种 (c.1772T>C p.(Leu591Ser)) 被确定.
- 预计这两种变体都会损害蛋白质的功能.
- 患者出现了严重的小牙,只剩下两个落叶犬.
结论:
- 鉴定的EVC2变种可能会协同加剧HED.中的寡类表型.
- 了解多个基因变异的影响对于解释HED表型中的个体差异至关重要.
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