ABHD5 and Dorfman-Chanarin disease: The mutationof ABHD5 gene causes the human Chanarin-Dorfman Syndrome or NeutralLipid Storage Disease with Ichthyosis (NLSDI), which is a rare autosomalrecessive disorder characterized by the presence of intracellularaccumulation of triacylglycerol (TG) droplets in many tissues.