Parajua J L, Goñi M, Giménez M, Feijóo M
Neurologia. 1989 Nov;4(9):333-5.
A family is reported with five generations showing hereditary chorea. In the youngest generation, two members had so severe choreic hyperkinesis that gait was impaired in one of them and totally impeded in the other; they also had associated mental retardation, which was not present in other members with variable degrees of hyperkinesis. There was no therapeutic response to several drugs. The literature regarding genetical, clinical and therapeutic aspects of this condition is reviewed, and it is concluded that the most adequate denomination for the disease is familial nonprogressive chorea rather that the accepted one of benign familiar chorea.
据报道,有一个家族五代人都表现出遗传性舞蹈病。在最年轻的一代中,两名成员患有严重的舞蹈性运动亢进,其中一人步态受损,另一人则完全无法行走;他们还伴有智力迟钝,而其他程度不同的运动亢进患者则没有这种情况。几种药物治疗均无效果。本文回顾了关于该病遗传、临床和治疗方面的文献,并得出结论,该病最恰当的名称应为家族性非进行性舞蹈病,而非目前公认的良性家族性舞蹈病。