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.diegojavierfares.com/mega-price-Houston-Texans-NFL-Side-Stripe-Training-Shorts-p6850-top-buy/