Yang Hua, Yang Jie, Xue Yawen, Liao Lihui, Cai Qianyun, Luo Rong
Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China.
Key Laboratory of Obstetric & Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education, Sichuan University, Chengdu, China.
Front Pediatr. 2024 Sep 27;12:1407341. doi: 10.3389/fped.2024.1407341. eCollection 2024.
Spinal muscular atrophy (SMA) is an autosomal recessive disease caused by mutations in the survival motor neuron 1 (SMN1) gene on chromosome 5, leading to the degeneration of lower motor neurons. There are few studies on cognitive impairment comorbid with SMA. Here, we report two cases of severe cognitive impairment in Chinese children with SMA type 1, marking the first such reports in this demographic. We propose that severe cognitive dysfunction may be a comorbidity of SMA. Clinicians should consider SMA in patients presenting with severe muscle weakness and atrophy accompanied by cognitive impairments, to avoid misdiagnosis and oversight.
脊髓性肌萎缩症(SMA)是一种常染色体隐性疾病,由5号染色体上生存运动神经元1(SMN1)基因的突变引起,导致下运动神经元变性。关于SMA合并认知障碍的研究很少。在此,我们报告了两例中国1型SMA患儿严重认知障碍的病例,这是该人群中的首例此类报告。我们提出严重认知功能障碍可能是SMA的一种合并症。临床医生在面对伴有认知障碍的严重肌肉无力和萎缩患者时应考虑到SMA,以避免误诊和漏诊。