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Ocular manifestations and management recommendations of lysosomal storage disorders I: mucopolysaccharidoses
The mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by inborn errors of glycosaminoglycan (GAG) metabolism. These diseases are classified by enzyme deficiency into seven groups: type I, II, III, IV, VI, VII, and IX. GAG accumulation leads to characteristic clinical feat...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567234/ https://www.ncbi.nlm.nih.gov/pubmed/26379420 http://dx.doi.org/10.2147/OPTH.S78368 |