Division of Pediatric Neurology, Department of Pediatrics, Faculty of Medicine, Ege University, İzmir, Turkey.
Pediatr Neurol. 2012 Mar;46(3):192-4. doi: 10.1016/j.pediatrneurol.2011.12.003.
Rett syndrome is a severe neurodevelopmental disease with a prevalence of 0.88 per 10,000 girls aged 5-18 years, and is often caused by mutations in methyl-cytosine-phosphate-guanine (CpG)-binding protein 2. Disorder of respiratory control is a prominent feature of Rett syndrome. Brainstem serotoninergic neurons are known to play an important role in the arrangement of breathing rhythm and pattern. We present a patient whose severe hyperventilation and apneic attacks resolved with the concomitant treatment of fluoxetine and buspirone. To our knowledge, we describe the first patient with Rett syndrome to receive fluoxetine for respiratory problems.
雷特综合征是一种严重的神经发育疾病,发病率为每 10000 名 5-18 岁女孩中有 0.88 名,通常由甲基胞嘧啶-磷酸-鸟嘌呤(CpG)结合蛋白 2 突变引起。呼吸控制障碍是雷特综合征的一个突出特征。已知脑干 5-羟色胺能神经元在呼吸节律和模式的排列中起重要作用。我们介绍了一位患者,其严重的过度通气和呼吸暂停发作在同时接受氟西汀和丁螺环酮治疗后得到缓解。据我们所知,我们描述了首例雷特综合征患者因呼吸问题接受氟西汀治疗的病例。