Vossler D G, Wyler A R, Wilkus R J, Gardner-Walker G, Vlcek B W
Epilepsy Center, Swedish Health Services, Seattle, WA 98122, USA.
Neurology. 1996 May;46(5):1258-61. doi: 10.1212/wnl.46.5.1258.
Norrie disease (ND) is an X-linked recessive disorder causing ocular atrophy, mental retardation, deafness, and dysmorphic features. Virtually absent monoamine oxidase (MAO) type-A and -B activity has been found in some boys with chromosome deletions. We report the coexistence of cataplexy and abnormal REM sleep organization with ND. Three related boys, referred for treatment of medically refractory atonic spells and apneas, underwent extended EEG-video-polysomnographic monitoring. They demonstrated attacks of cataplexy and inappropriate periods of REM sleep during which they were unarousable. One boy also had generalized tonic-clonic seizures. Previous testing revealed that all three have complete ND gene deletions. In all subjects, platelet MAO-B activity was absent, serum serotonin levels were markedly increased, and plasma catecholamine levels were normal. Data from the canine narcolepsy syndrome model implicate abnormal catecholaminergic and cholinergic activities in the pathogenesis of cataplexy. Our findings suggest that abnormal MAO activity or an imbalance between serotonin and other neurotransmitter levels may be involved in the pathogenesis of human cataplexy.
诺里病(ND)是一种X连锁隐性疾病,可导致眼部萎缩、智力迟钝、耳聋和畸形特征。在一些患有染色体缺失的男孩中发现几乎不存在单胺氧化酶(MAO)A 型和B型活性。我们报告了猝倒症和异常快速眼动睡眠组织与诺里病并存的情况。三名因治疗药物难治性无张力发作和呼吸暂停而前来就诊的相关男孩接受了长时间的脑电图-视频-多导睡眠图监测。他们表现出猝倒发作和快速眼动睡眠的不适当阶段,在此期间他们无法被唤醒。一名男孩还患有全身性强直-阵挛性癫痫发作。先前的检测显示,这三名患者均存在完整的诺里病基因缺失。在所有受试者中,血小板MAO-B活性缺失,血清5-羟色胺水平显著升高,血浆儿茶酚胺水平正常。来自犬发作性睡病综合征模型的数据表明,异常的儿茶酚胺能和胆碱能活动与猝倒症的发病机制有关。我们的研究结果表明,异常的MAO活性或5-羟色胺与其他神经递质水平之间的失衡可能参与了人类猝倒症的发病机制。