阵发性舞蹈手足徐动症的十年随访：一个散发病例转变为家族性病例。

Ten year follow-up of paroxysmal choreoathetosis: a sporadic case becomes familial.

作者信息

Bird T D, Carlson C B, Horning M

出版信息

Epilepsia. 1978 Apr;19(2):129-32. doi: 10.1111/j.1528-1157.1978.tb05022.x.

DOI:10.1111/j.1528-1157.1978.tb05022.x

Abstract

A 30-year-old woman is reported who was originally described in 1967 as an isolated instance of paroxysmal choreoathetosis. In the subsequent 10 years, her movement disorder has decreased in severity. However, she now has a 7-year-old daughter with a similar but more persistent and more serious condition. This family emphasizes both variability of manifestations of paroxysmal choreoathetosis and the importance of genetic factors.

摘要

据报道，一名30岁女性最初在1967年被描述为阵发性舞蹈手足徐动症的孤立病例。在随后的10年里，她的运动障碍严重程度有所减轻。然而，她现在有一个7岁的女儿，患有类似但更持续、更严重的疾病。这个家庭强调了阵发性舞蹈手足徐动症表现的变异性以及遗传因素的重要性。