双性功能丧失的EZH1变体会导致一种新的发育障碍,带有中部早发性青春期
Nobuhiko Okamoto1, Sayaka Yoshida2, Ayako Ogitani3
1Department of Medical Genetics, Osaka Women's and Children's Hospital, Izumi, Japan.
American journal of medical genetics. Part A
|May 30, 2024
概括
在EZH1的致病变体导致神经发育障碍. 这项研究报告说,双性EZH1变异的姐妹呈现发育延迟和早熟青春期,与韦弗综合征不同.
科学领域:
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 多镇压复合体-2 (PRC2) 对于发育至关重要,其变体会导致过度生长和神经系统疾病.
- EZH2,SUZ12和EED的致病变体与韦弗综合征和相关的过度生长/智力障碍 (OGID) 综合征有关.
- EZH1是EZH2的同源,也与PRC2的成分相互作用,最近与神经发育障碍有关.
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