Pantothenate kinase-associated neurodegeneration (PKAN), an autosomal recessive neurodegenerative disorder which used to known as the Halervorden-Spatz syndrome, is characterized by iron accumulation in the brain resulting in dystonia, choreoathetosis, rigidity, spasticity, tremor, dementia, or psychomotor retardation (Koeppen and Dickson, 2001). This evidence concerns the gene PANK1 and Dystonia.