AUTHOR=Starosta Rodrigo Tzovenos , Hou Ying-Chen Claire , Leestma Katelyn , Singh Prapti , Viehl Luke , Manwaring Linda , Granadillo Jorge Luis , Schroeder Molly C. , Colombo Jamie N. , Whitehead Halana , Dickson Patricia Irene , Hulbert Monica L. , Nguyen Hoanh Thi TITLE=Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations JOURNAL=Frontiers in Pediatrics VOLUME=10 YEAR=2022 URL=https://www.frontiersin.org/journals/pediatrics/articles/10.3389/fped.2022.944178 DOI=10.3389/fped.2022.944178 ISSN=2296-2360 ABSTRACT=
Infantile-onset Pompe disease (IOPD) is a rare, severe disorder of lysosomal storage of glycogen that leads to progressive cardiac and skeletal myopathy. IOPD is a fatal disease in childhood unless treated with enzyme replacement therapy (ERT) from an early age. Sickle cell anemia (SCA) is a relatively common hemoglobinopathy caused by a specific variant in the hemoglobin beta-chain. Here we report a case of a male newborn of African ancestry diagnosed and treated for IOPD and SCA. Molecular testing confirmed two