The objective is to track pregnancy outcomes in women with Pompe Disease and to follow
infants born to women with Pompe Disease.
Study Design Time Perspective: Retrospective and Prospective
- Enroll in or agree to enroll in Pompe Registry
- Be pregnant or have been pregnant with appropriate medical documentation
- Provide a signed Patient Information and Authorization Form to participate in the
sub-registry prior to any sub-registry related data collection is performed
- No Exclusion Criteria