Results of special neck exercises in a patient with cerebellar ataxia and axial myoclonus due to ADCK3 mutation

Özlem MENEVŞE

Cerebellar ataxia associated with the aarF-domain-containing kinase 3 (ADCK3) gene mutation is a hereditary type of ataxia related to autosomal recessivecerebellar ataxias. Additional symptoms, such as epileptic seizures, pyramidal signs, and myoclonus, may be seen in this progressive ataxia. This case reportaimed to present the results of the physiotherapy and rehabilitation program of a 19-year-old patient with cerebellar ataxia and myoclonus, due to coenzyme Q10deficiency, associated with the ADCK3 gene mutation. International cooperative ataxia rating scale, mini-mental state examination, ...Daha fazlası