Angelini L, Nardocci N, Rumi V, Lamperti E
Istituto Neurologico, C. Besta, Milan, Italy.
J Neurol. 1989 Sep;236(6):319-21. doi: 10.1007/BF00314372.
The natural history of early-onset idiopathic dystonia was studied in 30 patients. Worsening of motor symptoms was observed in the early stages, followed by spontaneous stabilization. Most of the patients retained functional independence. None showed mental deterioration, mood alteration or personality disturbance.
对30例早发性特发性肌张力障碍患者的自然病史进行了研究。在疾病早期观察到运动症状恶化，随后症状自发稳定。大多数患者保持功能独立。无一例出现智力衰退、情绪改变或人格障碍。
