Mutations in the PLA2G6 gene (Entrez GeneID:8398) have been identified in autosomal recessive neurodegenerative diseases classified as infantile neuroaxonal dystrophy (INAD), neurodegeneration with brain iron accumulation (NBIA), and dystonia-parkinsonism [1]–[3]. Here, PLA2G6 is linked to neurodegeneration with brain iron accumulation 2A.