Infantile neuroaxonal dystrophy (INAD) constitutes a rare neurodegenerative disorder associated with PLA2G6 gene mutation that exhibits a diverse spectrum of clinical presentation starting between six months and three years of age, characterized by progressive psychomotor regression, hypotonia, and gradually worsening stiffness in all limbs. Here, PLA2G6 is linked to neurodegeneration with brain iron accumulation 2A.