Hurler syndrome is a rare, inherited disease of metabolism in which a person cannot break down long chains of sugar molecules called socioeconomically. Some symptoms of Hurler syndrome often appear between ages 3 and 8. A young child with severe Hurler syndrome appear normal at birth. Facial symptoms may become more noticeable during the first 2 years of life. The day to day struggles of having this unfortunate disease is he decline of mental functioning, loss of physical skills, heart problems which include changes in their valves, Hearing problems an a high chance of ear infections, Deformed bones and stiff joints, especially the spine, hips, knees, wrists, and fingers, they are also short sized compared to a normal person and lastly they have breathing problems.