PLA2G6-associated neurodegeneration (NBIA/DYT/PARK-PLA2G6) comprises a continuum of three phenotypes with overlapping clinical and radiologic features: infantile neuroaxonal dystrophy (INAD), atypical neuroaxonal dystrophy (atypical NAD), and PLA2G6 -related dystonia-parkinsonism. The gene discussed is PLA2G6; the disease is Dystonia.