一个De Novo 8q22.2q22.3发育迟缓和先天性缺陷的女孩的间歇性微切除
Ruta Kalinauskiene1, Deimante Brazdziunaite2, Neringa Burokiene3
1Faculty of Medicine, Vilnius University, 01513 Vilnius, Lithuania.
Medicina (Kaunas, Lithuania)
|June 28, 2023
概括
这项研究详细介绍了一名患有8q22.2q22.3微切除的新患者,扩大了已知的临床特征. 放射性突突结还与这种罕见的遗传疾病有关.
科学领域:
- 遗传学 遗传学 是一个
- 人类表型研究 研究人类表型研究
背景情况:
- 间歇性 de novo 8q22.2q22.3 微切除是罕见的,以前只报告了九例.
- 这项研究旨在描述新患者的表型,并将其与现有文献进行比较,以完善对这种微删除综合征的理解.
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