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- W2563875567 abstract "Mucopolysaccharidosis type II (MPS II) is caused by deficiency of lysosomal enzyme iduronate-2-sulfatase. Insufficient activity of the enzyme results in accumulation of glycosaminoglycans leading to progressive multisystem pathologies. MPS II is less likely to be complicated by kidney and urinary tract problems. We report a boy with MPS II, who developed left hydronephrosis. His hydronephrosis improved after starting enzyme replacement therapy. It was suggested that MPS II was closely associated with the pathogenesis of hydronephrosis." @default.
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- W2563875567 date "2017-03-01" @default.
- W2563875567 modified "2023-09-24" @default.
- W2563875567 title "Resolution of Hydronephrosis in a Patient With Mucopolysaccharidosis Type II With Enzyme Replacement Therapy" @default.
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- W2563875567 doi "https://doi.org/10.1016/j.urology.2016.12.010" @default.
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