“…Within the spectrum of iron deposition disorders there is a group of genetic diseases that have in common a syndrome of NBIA [32,84,85,86]. These disorders include pantothenate kinase-associated neurodegeneration (PKAN, previously known as Hallervorden-Spatz syndrome) [87,88,89,90], PLA2G6 calcium-independent phospholipase A2 (PLAN) [91,92], infantile neuroaxonal dystrophy (INAD) [93,94], mitochondrial membrane protein-associated neurodegeneration (MPAN) [95,96,97,98], beta-propeller protein-associated neurodegeneration (BPAN) [99,100], CoA synthase protein-associated neurodegeneration (CoPAN) [101,102,103], fatty acid-2 hydroxylase-associated neurodegeneration (FAHN) [104,105], Kufor–Rakeb disease [106,107,108], aceruloplasminemia [109,110] and neuroferritinopathy [111,112].…”