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Health Care Professionals 
The Pompe Registry is an ongoing, observational database that tracks natural history and outcomes of patients with Pompe disease.
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Patients & Families 
The Pompe Registry is an important program that Genzyme sponsors and administers. A disease registry contains medical information on patients with a specific condition, in a database that can be analyzed and used by physicians treating patients with the same condition. Registries have proven to be especially valuable in rare diseases like Pompe disease. The collective information from the Registry is used to increase the understanding of the disease and to monitor patients over time, with the ultimate goal of improving the clinical outcomes of patients.
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 Health Care Professionals 

Forgot your password?
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Physician Online Enrollment

Participation in the Pompe Registry is open to all physicians managing patients
with Pompe disease. Physician enrollment in the Registry is simple. Complete the Physician Enrollment Form
by clicking on the link below.

Online Physician Enrollment
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