MSMDS is caused by a rare genetic mutation. It affects muscles that operate largely involuntarily in healthy people, including some in organs like the bladder, intestines and lungs.
EAU CLAIRE, Wis. - A 4-year-old Wisconsin boy is part of a unique group of people for a heartbreaking reason. He is one of only 60 people around the world to be diagnosed with a rare genetic disease.
Round after round of tests revealed Levi has multisystemic smooth muscle dysfunction syndrome, or MSMDS. Experts say only 60 people in the world have ever been diagnosed with the disease. It’s been challenging for the entire family, with Levi’s parents spending most of their time at home with their kids.
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