Treatment Options

Disease management strategies may include medications and lifestyle approaches to symptom relief, as well as interventions to delay serious complications due to muscle deterioration.

Enzyme Replacement Therapy (ERT)

Patients with Pompe disease have deficient or absent acid alpha-glucosidase (GAA) activity. ERT provides an exogenous source of GAA.

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Genzyme Medical Information can answer questions about Pompe disease.

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Schedule of Assessments

The Pompe Registry has developed a recommended schedule of assessments to help in the care and monitoring of patients with Pompe disease.

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Pompe Registry

Find out about the Pompe Registry, an ongoing, observational database that tracks natural history and outcomes of patients with Pompe disease.

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