Mucopolysaccharidosis Conditions Explained
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YouTubeCheckRare
Mucopolysaccharidosis Conditions Explained
Barbara Burton, MD, of Northwestern University Feinberg School of Medicine, provides an overview of the various mucopolysaccharidosis (MPS) conditions. The MPSs are a group of lysosomal storage disorders that include MPS I (e.g., Hurler syndrome), MPS II (Hunter syndrome), MPS III (Sanfilippo syndromes), MPS IV (Morquio syndrome), MPS VI ...
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Video: Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD) - Video Explanation! | Osmosis | 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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