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From the Community
Kyle's Blog
A teen with Hunter syndrome shares his story with his video blog.
Read Kyle's Blog
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Featured Resource
The National MPS Society supports families and individuals affected by MPS and related diseases. They work to advance scientific research and increase public and professional awareness of MPS.
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Connect with the Hunter Parents Community
The Hunter Parents community presents a unique opportunity to connect with other Hunter Parents. Together, parents can empower each other by exchanging knowledge, insights and stories!
Welcome to HunterPatients!
Hunter syndrome, or mucopolysaccharidosis II (MPS II) is a serious genetic disorder that primarily affects males. Hunter syndrome is one of several related lysosomal storage diseases. It interferes with the body's ability to break down and recycle specific mucopolysaccharides (mew-ko-pol-ee-sak-ah-rides).
This website is for people with Hunter syndrome, their family and friends, and healthcare providers.
For Healthcare Providers
Are you a Healthcare provider looking for more information about Hunter syndrome? Please visit our Healthcare Providers section for specialized information for different medical specialties. Read More
Resources
There are many helpful organizations that provide support for families managing Hunter syndrome. Whether you are looking for advocacy groups, government programs, or community support, explore some of the valuable resources here to help. Learn More
US/HUN-00103
