The FCMD gene encodes Fukutin, and FCMD is a genetic disease that is caused by an autosomal recessive mutation in the 10-exon of the FCMD gene, leading to muscle weakness, hypotonia, mental retardation, and meningitis in infancy [6,8,9,10]. The gene discussed is FKTN; the disease is Congenital muscular dystrophy, Fukuyama type.