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New rare disease platform launched for Hunter Syndrome

Read time: 1 mins
Last updated:1st Feb 2018
Published:1st Feb 2018
Source: Pharmawand

Hunter syndrome (MPS II) is a rare condition resulting from mutations in the gene that codes for the production of the lysosomal enzyme iduronate-2-sulfatase (I2S). Recognition and diagnosis at an early stage is crucial to establishing appropriate management strategies.

Please note the Hunter Syndrome Knowledge Centre is not intended for HCPs in USA or UK. It has been developed by EPG Health for, in collaboration with Shire.  

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