含有激酶 (TBCK) 的TBC1域的突变与相关的智力障碍和低位症
Prem Chand1, Asna Sulaiman2, Salman Kirmani1
1Department of Paediatrics and Child Health, Aga Khan University Hospital, Karachi, Pakistan.
JPMA. The Journal of the Pakistan Medical Association
|October 25, 2023
概括
婴儿低位症与精神运动迟缓和特征性Facies-3 (IHPRF-3) 综合征是TBCK基因突变的结果. 发现了一种新的功能丧失变异 (p.Gln164*),进步了对这种罕见的神经发育障碍的理解.
科学领域:
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
- 罕见疾病 罕见疾病
背景情况:
- 婴儿低血压与精神运动迟缓和特征性Facies-3 (IHPRF-3) 综合征是一种罕见的神经发育障碍.
- 它是由含有激酶 (TBCK) 基因的TBC1域中的突变引起的.
关键词:
婴儿低血压,智力障碍,基因突变.相关概念视频
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