由LAMA5基因中的复合异合突变引起的具有扩散性中性硬化症的先天性性综合征
Bobbity Deepthi1, Ramge Ramachandran Sivakumar1, Sudarsan Krishnasamy1
1Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, 605006, India.
Pediatric nephrology (Berlin, Germany)
|November 20, 2023
概括
在患有先天性性综合征的婴儿身上发现了LAMA5基因的遗传变异. 这一发现扩大了已知的扩散性中性硬化症的遗传原因.
科学领域:
- 遗传学 是一个遗传学.
- 儿科 儿科 儿科
- 腎臟病學 (nephrology) 是一種醫學專業.
背景情况:
- 先天性病综合征 (CNS) 是一种严重的脏疾病.
- 扩散性中性硬化症 (DMS) 是一种组织学发现,通常与中枢神经系统有关.
- 遗传因素在中枢神经系统和体质神经系统的发病过程中起着至关重要的作用.
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