Sfaihi Ben Mansour L, Ayedi A, Chaari W, Aloulou H, Kammoun T, Mnif Z, Mahfoudh A, Triki C, Hachicha M
Service de pédiatrie, CHU Hedi Chaker, 3029 Sfax, Tunisie.
Arch Pediatr. 2008 Jul;15(7):1197-200. doi: 10.1016/j.arcped.2008.04.005. Epub 2008 May 27.
Moyamoya syndrome has rarely been reported in association with Down syndrome. We report on 2 cases in 3-year-old and 6-year-old female children with Down syndrome, who presented with neurological deficit. Imaging (magnetic-resonance angiography and digital-subtraction angiography) revealed the classical Moyamoya pattern. The neurological deficits persisted in both cases. One patient has developed epilepsy.
烟雾综合征与唐氏综合征相关的报道极为罕见。我们报告了2例分别为3岁和6岁患有唐氏综合征的女童,她们均出现了神经功能缺损症状。影像学检查(磁共振血管造影和数字减影血管造影)显示出典型的烟雾病模式。两例患者的神经功能缺损症状均持续存在。其中一名患者已发展为癫痫。