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Mucopolysaccharidosis Illustration and Icon
Mucopolysaccharidosis
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A clinical illustration of a pediatric human exhibiting coarse facial features and a mildly protuberant abdomen, characteristic of a lysosomal storage disorder. In medical genetics, pediatrics, and pathology, mucopolysaccharidosis (MPS) is a genetic metabolic disease at the lysosome–cell level that impairs glycosaminoglycan degradation, affecting connective tissue and the musculoskeletal system across organ systems. The figure represents a systemic disease entity used for diagnostic teaching in Homo sapiens (human).
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