在一个神经眼心产尿综合征病例中,WDR37的剪接变异
Mai Samejima1, Mitsuko Nakashima2, Jun Shibasaki3
1Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan; Department of Pediatrics, Tokyo Metropolitan Ebara Hospital, Tokyo, Japan.
Brain & development
|December 3, 2023
概括
这项研究确定了WDR37基因中的一种新型拼接变异,导致神经眼心产尿综合征 (NOCGUS). 这些发现扩大了这种罕见遗传疾病的已知的表型谱.
科学领域:
- 遗传学和分子生物学
- 人类遗传学 人类遗传学
- 罕见疾病 罕见疾病
背景情况:
- 神经眼心血管发尿综合征 (NOCGUS) 是一种多系统性疾病,与WDR37基因变异有关.
- 以前的报道将误解变体与NOCGUS联系在一起,其特点是神经,眼睛和心脏问题.
研究的目的:
- 在受影响的患者中确定NOCGUS的遗传原因.
- 描述新型WDR37变种及其功能后果.
- 扩大对NOCGUS表型变异性的理解.
主要方法:
- 基因分析以确定WDR37变种.
- 拼接AI对拼接异常的预测.
- 通过RT-PCR来确认mRNA拼接缺陷.
- 患者的临床表型.
主要成果:
- 鉴定出一种新的内部WDR37删除 (c.727-27_727-24del).
- 删除导致异常拼接与内置保留和异常的氨基酸插入.
- 这位患者出现智力障碍,,小脑异常,结肠瘤,门缩和多囊.
结论:
- 这是首次报告由WDR37拼接变体引起的NOCGUS.
- 鉴定到的变异导致了明显的表型特征,包括新的特征.
- 这些发现扩大了WDR37相关的NOCGUS表型的范围.
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