Hunter syndrome

Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a rare inherited lysosomal storage disease in which large sugar molecules called glycosaminoglycans (or GAGs or mucopolysaccharides) build up in body tissues. Hunter syndrome is caused by a deficiency of the lysosomal enzyme iduronate-2-...

1 story • Updated Oct 14, 2025
Hunter syndrome
Health

FDA Extends Review Period for Denali's Hunter Syndrome Treatment

5 sources Oct 13, 2025