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2009•European Ophthalmic ReviewOpen access

Clinical Presentations of Treatable Lysosomal Storage Disorders – Gaucher, Fabry and Pompe disease and Mucopolysaccharidosis I

Susan A. Graham, Genzyme Europe BV, Naarden, The Netherlands

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Key concepts: Lysosomal storage disorders, Mucopolysaccharidosis, Fabry disease, Medicine, Mucopolysaccharidosis I, Enzyme replacement therapy, Lysosomal storage disease, Disease

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Clinical Presentations of Treatable Lysosomal Storage Disorders – Gaucher, Fabry and Pompe disease and Mucopolysaccharidosis I — Research Paper | ScholarLens