一个患有结核性硬化症的孩子具有新NRAS基因突变
P N Liveinai1, Neeraj Kumar1, Jyoti Kadian1
1Department of Pediatrics, Pandit Bhagwat Dayal Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India.
Journal of family medicine and primary care
|August 15, 2025
概括
结核性硬化症 (TS) 是一种罕见的遗传性疾病. 在患有TS的婴儿身上发现了一种新的NRAS基因突变,这表明与努南综合征-6的潜在联系.
科学领域:
- 遗传学 是一个遗传学.
- 神经学 神经学
- 儿科 儿科 儿科
背景情况:
- 结核性硬化症 (TS) 是一种罕见的自体主导遗传性疾病.
- 在TSC1或TSC2基因的突变导致多个器官的hamartomas.
- 这种TS会影响大脑,心脏,脏,皮肤,肺部和肝脏.
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