Dopa 반응성 근긴장이상증 -증례 보고-

Abstract

Dystonia is a rare syndrome of sustained muscle contractions which frequently causes twisting and repetitive movements or abnormal postures. Dopa-responsive dystonia(DRD) is a slowly progressive dystonia with childhood onset. Initial gait disturbance with toe-walking, diurnal variation of symptoms, dramatic response to levodopa treatment and concurrent signs of parkinsonism are other characteristics of DRD.

We report a 22 year old woman who showed the typical characteristics of DRD and was successfully managed with medical, surgical and rehabilitational methods. Better understanding of the disease entity and its treatment options are necessary for comprehensive rehabilitational management of DRD.