案例报告:LAMA2基因的新型框架转移突变导致1A型先天性肌肉衰竭
Natalia Diaz-Lombana1, Lorena Diaz-Ordoñez1,2, Juan David Gutierrez-Medina1,3
1Centro de Investigaciones en Anomalías Congénitas y Enfermedades Raras (CIACER), Universidad Icesi, Cali, Colombia.
Frontiers in genetics
|July 7, 2023
概括
这项研究报告了哥伦比亚第一个遗传确认的先天性肌肉衰竭1A型 (CMD1A) 病例. 它确定了一种新的LAMA2基因变异,导致这种罕见的神经肌肉疾病.
科学领域:
- 遗传学 是一个遗传学.
- 神经学 神经学
- 罕见疾病 罕见疾病
背景情况:
- 1A型先天性肌肉发育不良 (CMD1A) 是一种罕见的,自体逆性神经肌肉疾病.
- 它是由LAMA2基因的突变引起的,导致外周低血压,肌肉衰弱,白质异常和肌酸酸酶 (CPK) 的升高.
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