Hereditary ferritinopathy (HF) or neuroferritinopathy is an autosomal dominant, adult onset neurodegenerative disease caused by mutations in the ferritin light chain (FTL) gene (Curtis et al., 2001; Vidal et al., 2004a; Mancuso et al., 2005; Ohta et al., 2008; Devos et al., 2009; Kubota et al., 2009). This evidence concerns the gene FTL and neurodegenerative disease.