The purpose of this module is to raise awareness of the symptoms and natural history of the mucopolysaccharidoses (MPS), a group of rare lysosomal storage diseases, and to improve the index of suspicion for these disorders to ensure earlier diagnosis and intervention.

We share two case studies, one paediatric and one adult, to illustrate the typical clinical symptoms and available treatments for two types of MPS.

Published: March 8, 2021

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