Comparison of growth dynamics in different types of MPS: an attempt to explain the causes

Abstract Background Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by deficient activity of enzymes responsible for the catabolism of glycosaminoglycans (GAGs), resulting in progressive damage to various tissues and organs. Affected individuals present with skeletal de...

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Bibliographic Details
Main Authors: Agnieszka Różdżyńska-Świątkowska, Anna Zielińska, Anna Tylki-Szymańska
Format: Article
Language:English
Published: BMC 2022-09-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:https://doi.org/10.1186/s13023-022-02486-4