与Lennox-Gastaut综合征相关的ATP6V1B2相关疾病:基于病例的概述
Greta Amore1, Elisa Calì2, Maria Spanò3
1Department of Neuromuscular Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom; Unit of Child Neurology and Psychiatry, Department of Human Pathology of the Adult and Developmental Age "Gaetano Barresi", University of Messina, Via C. Valeria 1, 98125 Messina, Italy.
Brain & development
|August 26, 2023
概括
一个新的ATP6V1B2基因变体在患有全球发育迟缓和性脑病变的患者中被发现. 这一发现扩大了已知的ATP6V1B2相关疾病的范围,包括发育性脑病变.
科学领域:
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
- 神经学 神经学
背景情况:
- ATP6V1B2编码了参与器官酸化和细胞功能的溶酶体质子子单元.
- ATP6V1B2变种与具有可变神经参与的多系统性疾病有关.
- 有限的病例报告阻碍了对ATP6V1B2相关疾病中的基因型-表型相关性的理解.
研究的目的:
- 报告ATP6V1B2基因中的新型变异.
- 扩大对ATP6V1B2相关疾病的表型和分子谱的理解.
主要方法:
- 进行了整个外体序列测序.
- 分析了一个18岁男性患者的病例研究,该患者患有全球发育迟缓,骨异常和脑病变.
主要成果:
- 在ATP6V1B2中发现了一种新的de novo变异 (c.973G>C,p.Gly325Arg).
- 该患者呈现出全局发育迟缓,骨异常和伦诺克斯-加斯托综合征 (LGS).
结论:
- 发育性性脑病变 (DEE) 应考虑在与ATP6V1B2相关的疾病的范围内.
- 这一案例扩大了已知的ATP6V1B2相关疾病的临床和遗传景观.
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