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Updated: Jul 11, 2025

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三重症22:第一和第二季度细胞遗传学分析和表型表现在一系列七个案例
Chris Minella1, Eric Jeandidier2, Antoine Koch1
1Department of Maternal Fetal Medicine, Strasbourg University Hospital, Strasbourg, France.
Fetal diagnosis and therapy
|November 5, 2023
概括
在产前诊断的三形22 (染色体疾病) 是罕见的. 早期的产前数据可以指导对受影响的新生儿和家庭的护理.
科学领域:
- 遗传学 遗传学是一种遗传学.
- 产前诊断 在产前诊断
- 染色体异常 染色体异常
背景情况:
- 三胞胎瘤22是一种罕见的染色体疾病,不常见的产前检测.
- trisomy 22 的活产通常涉及受限的胎盘马赛克或真正的胎儿马赛克.
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