Todays spotlight is on Myoclonic dystonia Myoclonic Dystonia is better known as DTY11, myoclonus-dystonia, or according to the updated nomenclature DYT-SGCE, is characterized by rapid, involuntary, jerking movements (myoclonus) with or without sustained dystonic postures. Myoclonus most often affects the neck, trunk, and upper arms. Less commonly, the legs are … Continue reading →

Todays spotlight is on Paroxysmal kinesigenic dyskinesia (PKD) PKD is also known as PxMD-PRRT2 (previously named DYT10), is characterized by episodes of dystonia and choreoathetosis that are triggered by sudden movements or when startled. Episodes usually last seconds or minutes. In some cases, as many as 100 episodes can occur … Continue reading →

Todays spotlight on Dystonia is Paroxysmal nonkinesigenic dyskinesia (PKND) PKND is a disorder characterized by episodes of dystonia and choreoathetosis. Choreoathetosis is characterized by irregular, rapid, jerky movements that may occur in association with slow, writhing motions. Episodes may last from minutes to hours and can recur multiple times per … Continue reading →

Today’s spotlight on Dystonia is… Dopa-responsive dystonia (DRD) DRD is a general term for a few disorders in which generalized dystonia and Parkinsonism are present and often dramatically respond to treatment with levodopa. Levodopa is an amino acid that is converted to dopamine. Dopamine is a brain chemical that serves … Continue reading →