Different Mucopolysaccharidosis Disorders and Their Treatment Plans

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2025-08-27 08:02:48 -

Mucopolysaccharidosis (MPS) constitutes a spectrum of uncommon, hereditary lysosomal storage diseases stemming from inadequate enzyme production necessary for glycosaminoglycan (GAG) degradation. The excessive GAG buildup triggers systematic deterioration across multiple organ systems, skeletal framework, and cellular tissues. Enhanced comprehension of mucopolysaccharidosis causes continues...

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