Professor Kathryn Peall, a leading expert in myoclonus dystonia from Cardiff University, discusses the complexities of this condition, touching on both motor and non-motor symptoms. She sheds light on the genetic factors, particularly the role of the SGCE gene, and how it affects clinical presentation. The conversation also highlights the effectiveness of deep brain stimulation (DBS) as a treatment, underlining its potential when applied early, especially in children. Peall emphasizes the need for a more nuanced understanding of the interplay between psychiatric issues and motor symptoms.
