在胎儿中发现的ACTA1的新型变异具有秋变形序列和皮质发育延迟的胎儿
Clara Martínez-Diago1, Irene Mademont-Soler2, Alexandra Bonmatí1
1Department of Maternal-Fetal Medicine, Hospital Universitari Dr Josep Trueta, Girona, Spain.
Prenatal diagnosis
|April 26, 2024
概括
由内马林肌病 (NM) 引起的胎儿无动症变形序列可以呈现出产前大脑异常. 发现了一种新的ACTA1基因变异,表明骨肌肉的α-actin.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 发展生物学 发展生物学
背景情况:
- 尼马林肌病 (NM) 是一种先天性肌肉疾病.
- 胎儿无动症变形序列 (FADS) 涉及严重的胎儿无动症和多重关节收缩.
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