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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2022-09-01
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Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-022-02486-4 |