Mucopolysaccharidosis VI
Introduction: Mucopolysaccharidosis VI (MPS VI) is the result of the absence of arylsulfatase B leading to the abnormal lysosomal accumulation of glycosaminoglycans. Two different phenotypes have been described to date, namely, rapidly progressive and slowly progressive. Aim: To present the evolutio...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
SciELO
2015-02-01
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| Series: | Journal of Inborn Errors of Metabolism and Screening |
| Online Access: | https://doi.org/10.1177/2326409814567130 |