HECW2基因突变:西综合症的罕见原因:一个病例报告
Ankit Kumar Meena1, Aakash Mahesan1, Gautam Kamila1
1Department of Pediatrics, Centre of Excellence and Advanced Research for Childhood Neurodevelopmental Disorders, Child Neurology Division, AIIMS, New Delhi, India.
Neurology India
|July 24, 2025
概括
一种新的HECW2基因突变导致婴儿性脑病,其特征是松动,眼睛偏差和. 用上腺皮质激素和修改的阿特金斯饮食治疗显示出改善神经发育结果的前景.
科学领域:
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
- 儿科 儿科 儿科
背景情况:
- 外基组测序已经确定了许多与婴儿性脑病变相关的新突变.
- HECW2基因突变与发育迟缓和早期发作的有关.
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