Mucopolysaccharidosis Type I (MPS I): Symptoms, Causes & Treatment

MPS I is a rare genetic disorder that affects multiple body systems and exists on a spectrum from severe (Hurler syndrome) to attenuated forms. Severe MPS I presents in infancy with rapid disease progression, while attenuated MPS I may not be diagnosed until late childhood. The disorder is caused by IDUA gene mutations, leading to glycosaminoglycans accumulation in various tissues. Learn more about MPS I, its symptoms, and available treatment options in this video. This video on MPS I is brought to you by NORD (National Organization for Rare Disorders). Read the full report here: https://rarediseases.org/videos/mucop...