A type of mucopolysaccharidosis arises due to insufficient levels of the enzyme arylsulfatase B. This leads to symptoms akin to those observed in Hurler’s syndrome, including facial feature coarsening, skeletal distortions, cardiac irregularities, and enlargement of the liver and spleen. However, in this form, the child’s intelligence level remains normal. Typically emerging during early childhood, the condition lacks a distinct treatment, and heart failure-related mortality often transpires between the ages of 20 and 30.