Mucopolysaccharidoses: early diagnostic signs in infants and children
Abstract Mucopolysaccharidoses (MPS) comprise a group of lysosomal disorders that are characterized by progressive, systemic clinical manifestations and a coarse phenotype. The different types, having clinical, biochemical, and genetic heterogeneity, share key clinical features in varying combinatio...
Main Authors: | Cinzia Galimberti, Annalisa Madeo, Maja Di Rocco, Agata Fiumara |
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Format: | Article |
Language: | English |
Published: |
BMC
2018-11-01
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Series: | Italian Journal of Pediatrics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13052-018-0550-5 |
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