Mucopolysaccharidosis (MPS) is a group of rare genetic disorders affecting roughly 1 in 25,000 births, yet its impact is profound. Caused by enzyme deficiencies, MPS leads to the buildup of complex sugars in cells, resulting in progressive damage to the heart, bones, brain, and other organs. Symptoms can vary widely — from stunted growth and joint stiffness to vision and hearing loss. While there’s no cure yet, enzyme replacement therapies and other mucopolysaccharidosis treatments can help manage symptoms and improve quality of life. Raising awareness is crucial — early diagnosis can make all the difference in the fight against MPS.
Types of Mucopolysaccharidosis
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