Infantile Pompe disease on ERT—Update on clinical presentation, musculoskeletal management, and exercise considerations - Case - 2012 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
About Pompe Disease - SaveChloe
Types of Pompe – Pompe Disease (Glycogen Storage Disease 2)
This child was treated for a rare genetic disease while in the womb
Crowdfunding to help fund Baby Caitlyn's Enzyme Replacement Therapy for a rare genetic metabolic disease called Infantile Pompe Disease. on JustGiving
Infantile-Onset Pompe Disease (IOPD) Clinical Study | Sanofi Studies
Cayden's Journey With Infant Pompe Disease | Carlisle PA
Orofacial features and pediatric dentistry in the long-term management of Infantile Pompe Disease children | Orphanet Journal of Rare Diseases | Full Text
Pompe disease: literature review and case series. - Abstract - Europe PMC
IJNS | Free Full-Text | Is Newborn Screening the Ultimate Strategy to Reduce Diagnostic Delays in Pompe Disease? The Parent and Patient Perspective
Divergent clinical outcomes of alpha-glucosidase enzyme replacement therapy in two siblings with infantile-onset Pompe disease treated in the symptomatic or pre-symptomatic state - ScienceDirect
Development of facial muscle weakness over time in Patient 1 (a, b) and... | Download Scientific Diagram