Mucopolysaccharidosis Type I (MPS I): Symptoms, Causes & Treatment
5:21
YouTubeNational Organization for Rare Disorders (NORD)
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 ...
840 viewsApr 1, 2025
Hurler syndrome Symptoms
Video: Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD) - Video Explanation! | Osmosis | Osmosis
Video: Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD) - Video Explanation! | Osmosis | Osmosis
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Aug 1, 2024
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD): Video, Causes, & Meaning | Osmosis
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Kennedy and her brother Lincoln have a rare disease called MPS1, hurler syndrome. MPS1 causes the body to not produce certain enzymes that are needed in the breakdown of the body’s garbage. Essentially, the garbage builds up with no garbage truck to take it out. This has an effect on every part of the body, shortening life expectancy. There is no cure for MPS1. Our mission is to raise awareness and find a cure. | The Kennedy Ladd Foundation, Inc.
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