Angelini L, Rumi V, Lamperti E, Nardocci N
Department of Child Neurology, Istituto Neurologico C. Besta, Milano, Italy.
Neuropediatrics. 1988 Nov;19(4):171-4. doi: 10.1055/s-2008-1052439.
A group of nine patients with paroxysmal non epileptic motor disorders, with onset in the first year of life, is presented. The characteristics of the attacks define them as paroxysmal dystonia. The progression of the symptoms showed a spontaneous remission in a short length of time (6-22 months) in most infants. In two of them the symptoms persist, showing, however, a progressive decrease. All the laboratory tests were normal. None of the subjects revealed neurological signs and psychomotor development was normal. A likely correlation between transient early-childhood paroxysmal dystonia and developmental processes is discussed.
本文报告了一组9例阵发性非癫痫性运动障碍患者，这些患者在出生后第一年起病。发作特征将其定义为阵发性肌张力障碍。多数婴儿症状进展显示在短时间内（6 - 22个月）自发缓解。其中2例症状持续存在，但呈进行性减轻。所有实验室检查均正常。所有受试者均未发现神经体征，精神运动发育正常。本文讨论了短暂性儿童期阵发性肌张力障碍与发育过程之间可能存在的相关性。
