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Ocular features in mucopolysaccharidosis: diagnosis and treatment
Mucopolysaccharidoses (MPS) are a group of rare lysosomal storage disorders characterized by the accumulation of glycosaminoglycans (GAGs) in different parts of the eye. Ocular problems are very common in MPS children, and the cornea, sclera, trabecular meshwork, retina, and optic nerve may all be i...
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| 出版年: | Ital J Pediatr |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6238255/ https://ncbi.nlm.nih.gov/pubmed/30442167 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-018-0559-9 |
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