The new frame for Mucopolysaccharidoses
Abstract Mucopolysaccharidoses (MPS) are genetic, progressive, lysosomal storage disorders affecting virtually all organs and systems. The first MPS were clinically identified about 100 years ago. Nowadays, the enzyme defects and related genes are known for all 11 different enzyme defects. Treatment...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2018-11-01
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| Series: | Italian Journal of Pediatrics |
| Online Access: | http://link.springer.com/article/10.1186/s13052-018-0549-y |