Hunter Syndrome, also known as Mucopolysaccharidosis II (MPS II), is a rare genetic disorder that affects the body's ability to break down long chains of sugar molecules called glycosaminoglycans (GAGs). As a result, GAGs accumulate in the body's tissues, causing a range of symptoms that can vary in severity. There is currently no cure for Hunter Syndrome, but several treatment options are available to manage its symptoms and improve the quality of life of those affected.
