MPS Disorders
The National MPS Society provides support to families and promotes research initiatives that affect the following disorders:
MPS I (Hurler, Scheie, Hurler-Scheie syndromes)
Click here to meet a special individual with MPS I.
Click here to download a resources that explains MPS I in detail.
MPS II (Hunter syndrome)
Click here to meet a special individual with MPS II.
Click here to download a resources that explains MPS II in detail
MPS III (Sanfilippo A, Sanfilippo B, Sanfilippo C, Sanfilippo D syndome)
Click here to meet a special individual with MPS III.
Click here to download a resources that explains MPS III in detail
MPS IV (Morquio A, Morquio B syndromes)
Click here to meet a special individual with MPS IV.
Click here to download a resources that explains MPS IV in detail
MPS VI (Maroteaux-Lamy syndrome)
Click here to meet a special individual with MPS VI.
Click here to download a resources that explains MPS VI in detail
MPS VII (Sly syndrome)
Click here to meet a special individual with MPS VII.
Click here to download a resources that explains MPS VII in detail
MPS IX (Hyaluronidase deficiency syndrome)
ML II/III (I-cell and Pseudo-Hurler Polydystrophy)
Click here to meet a special individual with ML II/III.
Click here to download a resources that explains ML II/III in detail
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MPS Disorders
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The Join the Search campaign is made possible by support from BioMarin Pharmaceutical Inc., Genzyme Corporation and Shire Human Genetic Therapies.