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Presentation and treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome)

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Published in 2017 at "Expert Opinion on Orphan Drugs"

DOI: 10.1080/21678707.2017.1296761

Abstract: ABSTRACT Introduction: Mucopolysaccharidosis Type II (MPS II; Hunter syndrome) is an X- linked lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS). IDS deficiency leads to primary accumulation of dermatan sulfate (DS) and heparan… read more here.

Keywords: mucopolysaccharidosis type; hunter syndrome; treatment; mps hunter ... See more keywords