 Open Access Case Report 
Article ID: OJPDT-1-102
                                                  
                        
Open Access Case Report 
Article ID: OJPDT-1-102                                    
                                    
                                    
                                    
                                    
									Dystonia is defined as a movement disorder characterized by involuntary muscular contractions that generate twisting and repetitive movements and/or abnormal postures [1]. The traditional clinical categorization of the dystonias based on age at onset, distribution of symptoms (focal, segmental, multifocal, generalized), and site of onset remains important and overlaps with the more recently employed genetic classification. Early-onset primary dystonia is a condition characterized by progressive problems with movement, typically beginning in childhood [2]. Early-onset dystonia often starts in a limb, tends to generalize and frequently has a genetic origin; whereas adult-onset dystonia usually spares the lower extremities, frequently involves cervical or cranial muscles with a tendency to remain focal, and appears sporadic in most cases [3].
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Published on: Jun 10, 2017 Pages: 27-29
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                                    													DOI: 10.17352/ojpdt.000002
                                    
                                    
                                   
 
 
 
                                    
                                    
                                    
                                                  
                                                    
                                                    
													 												
                                                     
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