Jan J E, Tingle A J, Donald G, Kettyls M, Buckler W S, Dolman C L
Dev Med Child Neurol. 1979 Oct;21(5):648-52. doi: 10.1111/j.1469-8749.1979.tb01680.x.
This report describes the clinical course of a 16-year-old Canadian-born Chinese boy who has progressive rubella panencephalitis. The progression, the lack of response to 'Isoprenosine', and the additional finding of myopathy are discussed. The clinical and pathological features of this rare, progressive neurological disorder are also summarized. In view of the last major rubella pandemic occuring in the mid-60s, it is likely that during the next few years physicians will diagnose an increased number of patients with this distinct neurological entity.
本报告描述了一名16岁出生于加拿大的华裔男孩患进行性风疹全脑炎的临床病程。讨论了病情进展、对“异丙肌苷”缺乏反应以及发现的肌病。还总结了这种罕见的进行性神经疾病的临床和病理特征。鉴于上一次大规模风疹疫情发生在60年代中期，未来几年医生可能会诊断出更多患有这种独特神经疾病的患者。
