| Literature DB >> 29627187 |
Mrudu Herbert1, Heidi Cope1, Jennifer S Li2, Priya S Kishnani3.
Abstract
Based on a review of a large patient cohort, published literature, and 3 newborn screening cohorts, we concluded that children diagnosed through newborn screening with late-onset Pompe disease and the common heterozygous c.-32-13T>G variant require frequent cardiac follow-up with electrocardiography for arrhythmias. However, there is limited evidence for performing repeated echocardiography for cardiomyopathy.Entities:
Keywords: acid-α-glucosidase; arrhythmia; glycogen storage disease type II; hypertrophic cardiomyopathy
Mesh:
Substances:
Year: 2018 PMID: 29627187 DOI: 10.1016/j.jpeds.2018.02.007
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406