新型变异CPLANE 1:c.5051C>A (p.Ser1684Ter) 在患有朱伯特综合征的印度新生儿中
Saikat Patra1, Garima Goyal1, Yasir Ahmad Lone2
1Neonatology, Himalayan Institute of Medical Sciences, Dehradun, Uttarakhand, India.
BMJ case reports
|May 31, 2023
概括
朱伯特综合征 (JS) 是一种罕见的遗传疾病. 这一案例突出了印度新生儿的新奇CPLANE1基因突变,扩大了对JS的遗传理解.
科学领域:
- 遗传学 是一个遗传学.
- 神经学 神经学
- 发育生物学 发展生物学
背景情况:
- 朱伯特综合征 (JS) 是一种罕见的纤毛病,其特征是低血压,发育迟缓,以及大脑MRI上的牙标志 (MTS).
- 下一代测序已经确定了约35个导致JS的基因,CPLANE1突变占病例的8-10%.
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