The actual frequency of VLDLR-associated cerebellar hypoplasia is unknown, but initial reports regarded not more than twenty-five affected individuals in Canada and USA [113,252], although the condition occurs worldwide, PAFAH1B1-associated lissencephaly is very rare as the prevalence of classic lissencephaly ranges from 11.7 to 40 per million births [120]. The gene discussed is PAFAH1B1; the disease is Cerebellar hypoplasia.