Mucopolysaccharidosis

Mucopolysaccharidosis (MPS) refers to a group of inherited disorders caused by the body’s inability to break down certain complex carbohydrates called glycosaminoglycans (GAGs). These substances accumulate in cells, leading to progressive damage in various organs and tissues. Symptoms vary but may include skeletal abnormalities, heart problems, and developmental delays. MPS is typically diagnosed in childhood and can affect physical and cognitive abilities. Treatment options include enzyme replacement therapy and supportive care to manage symptoms, but there is currently no cure. Early diagnosis and intervention are crucial for improving quality of life.