Subtle Symptoms of a Rare Disease – Mucopolysaccharidosis I (MPS I)
Mucopolysaccharidosis I (MPS I) is a rare inherited genetic disorder caused by a deficiency of an enzyme, α-L-iduronidase, leading to a buildup of a waste product called glycosaminoglycans (GAGs). Dr. Lynda Polgreen, Pediatric Endocrinologist and Assistant Professor of Pediatrics at the Geffen School of Medicine at UCLA will help you recognize the symptoms of MPS I, a rare genetic disease, and shorten the diagnostic journey for patients with MPS I. This video is sponsored by Sanofi Genzyme. SAUS.MPSI.18.05.3222a
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