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MPS I is a progressive disease. Early diagnosis and intervention may prevent irreversible damage.
In this section, you will find information on:
In MPS I, glycosaminoglycan (GAG)-engorged cells accumulate and displace healthy normal cells in tissue and organs such as the liver and spleen, causing a host of signs, including skeletal deformities, coarse facial features, and an enlarged liver and spleen.
Meet Denise, a 40-year-old woman with MPS I who enjoys her life to the fullest.