Junqueira Paulo Alves, Moura-Ribeiro Maria Valeriana L de
Departamento de Neurologia, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brasil.
Arq Neuropsiquiatr. 2002 Jun;60(2-A):274-80.
We present a clinic-epidemiological study of two patients and meta-analysis (period 1977-2000 ) of the co-morbidity of the Down syndrome (DS) and moyamoya syndrome (MMS). Among the 42 patients listed in this survey, meta-analysis permitted to find the highest number of publications by researchers from Japan and United States, followed by Brazil and Italy; prevalence of cerebrovascular disease in suckling and pre school children; first symptomatology was hemiparesis (78.6%), speech disorders (26.2%); ischemic infarction (76.2%); recurring ischemic episodes (62%); bilateral impairment (83.3%). This analysis led to the conclusion that in the clinic-neurological investigation of DS patients with acute hemiparesis episodes, MMS should be included as the most probable diagnosis.
我们开展了一项针对两名患者的临床流行病学研究,并对1977年至2000年期间唐氏综合征(DS)与烟雾病综合征(MMS)共病情况进行了荟萃分析。在本次调查列出的42名患者中,荟萃分析发现日本和美国的研究人员发表的相关论文数量最多,其次是巴西和意大利;婴儿期和学龄前儿童脑血管疾病的患病率;首发症状为偏瘫(78.6%)、言语障碍(26.2%);缺血性梗死(76.2%);反复缺血发作(62%);双侧损害(83.3%)。该分析得出结论,在对急性偏瘫发作的DS患者进行临床神经学检查时,应将MMS作为最可能的诊断纳入考虑。