Nausieda P A, Grossman B J, Koller W C, Weiner W J, Klawans H L
Neurology. 1980 Mar;30(3):331-4. doi: 10.1212/wnl.30.3.331.
To document possible changing characteristics of Sydenham chorea, we reviewed records of 240 patients with this diagnosis who were seen between 1951 and 1976. A dramatic progressive decline in the number of cases was observed. The syndrome occurred mainly in childhood. Female predominance was apparent only after the 10. There was a high femilial incidence for both chorea and rheumatic fever. Most patients had generalized chorea, and fewer than 20% had hemichorea. Dysarthria, probably of extrapyramidal origin, was frequent but neurologic abnormalities other than diffuse encephalopathy were rare. One-third of the patients had coexisting heart disease. Repeat attacks of Sydenham chorea occurred, but the recurrence rate was much less than noted in previous studies.
为记录 Sydenham 舞蹈症可能变化的特征,我们回顾了1951年至1976年间确诊的240例该疾病患者的记录。观察到病例数量急剧逐渐下降。该综合征主要发生在儿童期。女性优势仅在10岁以后明显。舞蹈症和风湿热的家族发病率都很高。大多数患者有全身性舞蹈症,不到20% 有偏侧舞蹈症。构音障碍可能源于锥体外系,很常见,但除弥漫性脑病外的神经学异常很少见。三分之一的患者同时患有心脏病。Sydenham 舞蹈症会复发,但复发率远低于先前研究中所指出的。