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Hunter syndrome is an inherited disorder where glycosaminoglycans (GAGs) build up in cells of the body due to a deficiency of the enzyme iduronate-2-sulfatase.
There is no cure for the syndrome and treatment is aimed at managing the condition so as to ease symptoms and provide some relief for the sufferer. This is referred to as palliative treatment and the objective is to minimize negative effects on bodily functions as the condition worsens.
Some emerging treatments have also been shown to help slow disease progression and decrease the severity of the syndrome.
Some of these treatments include: