Although NBIA syndromes are rare genetic disorders with classic Mendelian inheritance (mostly autosomal Recessive type), some pathologic mutations in NBIA genes have been reported in rare monogenic Mendelian inheritance cases of Parkinson disease like ATP13A2 and PLA2G6 gene that are assigned respectively as PARK9 and PARK14 gene. The gene discussed is PLA2G6; the disease is neurodegeneration with brain iron accumulation.