Clinical ocular manifestations of Taiwanese patients with mucopolysaccharidoses VI (Maroteaux–Lamy syndrome)

Mucopolysaccharidoses (MPS) is a group of lysosomal storage disorders that lead to accumulation of glycosaminoglycans (GAGs) in many tissues and organs, resulting in different clinical features. In this study, we conducted the manifestation changes of refractive error, corneal clouding, and intraocu...

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Detalles Bibliográficos
Autores principales: Lin, Hsu-Ying, Huang, You-Hsin, Lei, Shao-Yu, Chen, Lee-Jen, Lin, Shuan-Pei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759551/
https://www.ncbi.nlm.nih.gov/pubmed/31572657
http://dx.doi.org/10.4103/tjo.tjo_85_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759551/
https://www.ncbi.nlm.nih.gov/pubmed/31572657
http://dx.doi.org/10.4103/tjo.tjo_85_17

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