Various forms of Classical lissencephaly (also called type I lissencephaly) include anomalies in the LIS1 gene (isolated lissencephaly and Miller-Dieker syndrome (MDS), anomalies in the TUBA3 and DCX genes, and lissencephaly caused by mutations in the ARX gene (XLAG syndrome, X-linked lissencephaly with agenesis of the corpus callosum). The gene discussed is PAFAH1B1; the disease is lissencephaly type 1 due to doublecortin gene mutation.