About MPS I
Mucopolysaccharidosis type I (MPS I) is a rare genetic condition that affects many parts of the body. It happens because the body is missing an enzyme needed to break down certain sugars. Over time, these sugars build up and cause damage. MPS I can be severe or milder, and symptoms usually get worse as a person grows older.
MPS I can be found through newborn screening or when symptoms appear later in life. Early diagnosis is important because treatment works best when started early. With early diagnosis, proper treatment, and regular medical follow-up, people with MPS I can have better health outcomes and quality of life.
