Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) is a group of inherited genetic disorders that involve defects in enzymes that break down complex sugar molecules known as mucopolysaccharides. MPS causes progressive damage to the body’s organs, cells and tissues, leading to physical disability, shortened lifespan and other serious medical problems. Symptoms can include skeletal and joint deformities, hearing loss, vision problems, organ enlargement and enlargement of the liver and spleen. There is no cure for MPS, but early diagnosis and treatments, such as enzyme replacement therapy, can help manage symptoms. This can improve the quality of life for people with the condition.