Ouvrier R A
Ann Neurol. 1978 Nov;4(5):412-17. doi: 10.1002/ana.410040505.
Three children, 2 of them siblings, developed a progressive dystonic condition in the first decade of life. The symptoms and signs were milder in the mornings or after a daytime nap but worsened greatly later in the day. One patient became unable to walk by evening. Investigations in 2 patients revealed a reduced concentration of cerebrospinal fluid homovanillic acid. The 2 more severely affected patients showed dramatic and sustained improvement with levodopa therapy. The condition bears a clinical resemblance to some reported cases of juvenile Parkinson's disease but is probably a separate disorder.
三个孩子,其中两个是兄弟姐妹,在生命的第一个十年里出现了进行性肌张力障碍。症状和体征在早晨或白天小睡后较轻,但在当天晚些时候会大大加重。一名患者到晚上就无法行走了。对两名患者的检查发现脑脊液高香草酸浓度降低。两名受影响更严重的患者在左旋多巴治疗后表现出显著且持续的改善。这种病症在临床上与一些报道的青少年帕金森病病例相似,但可能是一种单独的疾病。