McKusick-Kaufman (MKS) syndrome is a rare. autosomal recessive disorder. determined by genetic mutation in the MKKS gene on chromosome 20. MKS commonly manifests with three primary components: Polydactyly. https://www.ngetikin.com/bargain-MLB-Texas-Rangers-Alternate-Away-Jersey-iPhone-14-Pro-Clear-Case-p111023-save-big/