Hunter Syndrome Basics

If you or someone you know has Hunter syndrome, one of the most important things you can do is learn about the disease. In this section, we provide information about Hunter syndrome, including the biochemistry and genetics.

After reading these pages, you may want to talk with your doctor about additional sources of information. Your doctor might refer you to other healthcare professionals such as a medical geneticist or genetic counselor, who can help you learn more about Hunter syndrome and how it may impact the lives of you and your family.

OnePathSM Services

OnePathSM is a great resource if you have questions about Hunter syndrome or about navigating through prior authorizations or other insurance related matters. You may contact OnePathSM at 1-866-888-0660 and onepath@shire.com. Case managers are available to answer your call from 8:30am-8:00pm ET.

Related Links

National Organization for Rare Disorders (NORD)

www.rarediseases.org

NORD is a unique federation of voluntary health organizations dedicated to helping people with rare "orphan" diseases and assisting the organizations that serve them. NORD is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and service.