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      Fatal Care Research Foundation


      Fatal Care Research Center inaugurated a support group for children affected with an inborn error of metabolism called Mucopolysaccharidosis on August 08, 2003. The support group also caters to children suffering from other Lysosomal Storage Disorders (LSDs) such as Gaucher, Pompe and Fabry diseases for which Enzyme Replacement Therapy is now available.

       

      Source: https://fcrf.org.in/mps_abus.asp
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      The symptoms of Mucopolysaccharidosis and the treatments that are available vary depending on which type of Mucopolysaccharidosis a patient has been diagnosed with. Select which type you want to learn more about, and can highlight the resources that are most relevant to your MPS/ML type.


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