National Hospital of Sri Lanka, Colombo, Sri Lanka.
Neuromuscular Disorders Group, Nuffield Department of Clinical Neurosciences, Weatherall Institute of Molecular Medicine, Oxford OX3 9DS, UK.
Neuromuscul Disord. 2021 Mar;31(3):246-248. doi: 10.1016/j.nmd.2020.12.002. Epub 2020 Dec 11.
Congenital myasthenic syndromes (CMS) are genetically determined heterogenous disorders of neuromuscular transmission. We report a rare mutation of COLQ causing CMS in an Asian man that remarkably improved with fluoxetine. A 51-year-old Sri Lankan man with slowly progressive fatigable muscle weakness since eight years of age, presented with type 2 respiratory failure that required mechanical ventilation in the acute crisis and subsequent home-based non-invasive ventilation. His birth and family histories were unremarkable. On examination, he had limb girdle type of muscle weakness with fatigability and normal tendon reflexes with no ocular or bulbar involvement. DNA sequencing revealed a pathogenic homozygous mutation in COLQ gene: ENST00000383788.10:exon16:c.1228C>T:p.R410W, the first report in an Asian. Treatment with fluoxetine resulted in remarkable improvement and regain of muscle power and independence from assisted ventilation.
先天性肌无力综合征(CMS)是一种遗传性神经肌肉传递障碍的异质性疾病。我们报告了一例 COLQ 基因突变导致 CMS 的亚洲男性病例,该患者使用氟西汀治疗后显著改善。一名 51 岁的斯里兰卡男性,自 8 岁起出现进行性疲劳性肌肉无力,在急性危象时需要机械通气,并随后在家中接受无创通气。他的出生和家族史无异常。检查时,他表现为肢体带型肌无力,伴有易疲劳性,腱反射正常,无眼或球部受累。DNA 测序显示 COLQ 基因存在致病性纯合突变:ENST00000383788.10:exon16:c.1228C>T:p.R410W,这是亚洲首例报道。氟西汀治疗后,肌肉力量显著改善,患者能够独立脱机。