案例报告:在一个发育迟缓和身材矮小的中国男孩身上发现了一种新的PRR12变异
Zhengxia Liu1, Shuxia Ding2, Guangwei Xu3
1Department of Neurology, Women and Children's Hospital Affiliated to Ningbo University, Ningbo, Zhejiang, China.
Frontiers in pediatrics
|May 27, 2024
概括
这项研究详细介绍了一名智力障碍和多动症的中国男孩的新型Proline Rich 12 (PRR12) 基因变异. 这些发现扩大了对PRR12变体和神经发育障碍的理解.
科学领域:
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
- 发育生物学 发展生物学
背景情况:
- 富于氨酸12 (PRR12) 蛋白主要存在于大脑的核中.
- PRR12基因变异与神经眼综合征有关,其特点是智力障碍 (ID),神经精神问题和先天性异常,有或没有眼睛异常.
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