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...

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Detalles Bibliográficos
Autores principales: Fenzl, Carlton R, Teramoto, Kyla, Moshirfar, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Review
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

Internet

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

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