– Jen, mother of child with MPS I
– Jen, mother of child with MPS I
Find Information and learn about living with MPS I disease.
Learn about the causes, diagnosis and management of MPS I disease.
MPS I disease is an inherited genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase. Globally, MPS I occurs in about 1 in every 100,000 births.
May 15th is International MPS Awareness Day. Join Sanofi Genzyme as we support raising awareness of MPS disease disorders and honoring the individuals and families who are affected.
