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...
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| 主要な著者: | , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMC
2018-11-01
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| シリーズ: | Italian Journal of Pediatrics |
| 主題: | |
| オンライン･アクセス: | http://link.springer.com/article/10.1186/s13052-018-0550-5 |
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