Centre de Référence des Maladies Neuromusculaires Grand Est (CERNEST), American Memorial Hospital, Reims, France.
Unité d'Explorations Fonctionnelles Pédiatriques, American Memorial Hospital, Reims, France.
J Clin Sleep Med. 2017 Sep 15;13(9):1105-1108. doi: 10.5664/jcsm.6734.
Selenoprotein-related myopathy (-RM) is a rare disease with a variable clinical presentation. The selenoprotein N1 gene () mutation causing this congenital muscular dystrophy was identified in 2001. Sleep-disordered breathing (SDB) may occur in young patients with -RM who are still able to walk. We report the cases of two children with -RM who presented with SDB at the ages of 7 and 12 years and for whom long-term nocturnal noninvasive ventilation yielded significant improvement. Based on literature review and our current cases, it seems that there is no obvious relationship between the time since SDB onset and outcome of pulmonary function tests or limb muscle weakness. We therefore suggest that SDB should be systematically screened for in patients with -RM, at regular intervals using nocturnal polysomnography.
硒蛋白相关肌病(-RM)是一种临床表现多变的罕见疾病。导致这种先天性肌营养不良的硒蛋白 N1 基因()突变于 2001 年被确定。睡眠呼吸障碍(SDB)可能发生在仍能行走的 -RM 年轻患者中。我们报告了两例 7 岁和 12 岁时出现 SDB 的 -RM 儿童的病例,他们接受长期夜间无创通气治疗后病情显著改善。基于文献回顾和我们目前的病例,似乎 SDB 发病时间与肺功能测试或肢体肌无力的结果之间没有明显关系。因此,我们建议应定期使用夜间多导睡眠图对 -RM 患者进行 SDB 的系统筛查。