Ono S, Kurisaki H
Department of Neurology, Teikyo University School of Medicine, Ichihara Hospital, Chiba, Japan.
J Neurol. 1988 Sep;235(7):397-9. doi: 10.1007/BF00314480.
Twin males aged 24 years showed dementia, dysarthria, gait disturbances and involuntary movements, with slightly low levels of serum copper and ceruloplasmin, and markedly low excretion of urinary copper. We propose that the unique combination of dementia, dysarthria, gait disturbances, involuntary movements and abnormalities of copper metabolism does not fit any known nosological entity and constitutes a "new" syndrome different from Wilson's and Menkes' diseases.
两名24岁的男性双胞胎出现痴呆、构音障碍、步态障碍和不自主运动,血清铜和铜蓝蛋白水平略低,尿铜排泄明显减少。我们认为,痴呆、构音障碍、步态障碍、不自主运动以及铜代谢异常的独特组合不符合任何已知的疾病分类实体,构成了一种不同于威尔逊病和门克斯病的“新”综合征。