WWOX and spinocerebellar ataxia type 12: Further genetic analysis using chromosomal microarray analysis or whole-exome sequencing identified biallelic pathogenic variants in WWOX in autosomal recessive neurological disorders: spinocerebellar ataxia type 12 (SCA12) accompanied by epilepsy and intellectual disability and childhood epileptic encephalopathy known as WWOX-related epileptic encephalopathy (WOREE) (Mallaret M., et al., 2014; Abdel-Salam G et al., 2014).