Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. [[DYT8]] (PNKD): This form is associated with paroxysmal nonkinesigenic dyskinesia and can include dystonic movements during episodes. Dystonia with Neurodegeneration: Some genetic forms of dystonia are associated with neurodegenerative features. [[DYT3]] ([[ATP1A3]]): Also known as rapid-onset dystonia-parkinsonism (RDP), this condition presents with abrupt onset dystonia and parkinsonism. It's important to note that genetic dystonias can be inherited in an autosomal dominant, autosomal recessive, or X-linked manner. Genetic testing is often employed to identify specific gene mutations associated with dystonia, providing valuable information for diagnosis and sometimes influencing treatment decisions dyt8.txt Last modified: 2024/06/07 02:52by 127.0.0.1