
																
																	Cardiac outcome in classic infantile Pompe disease after 13â¯years of treatment with recombinant human acid alpha-glucosidase
																
																
																
															Keywords: اسید آلفا گلوکوزیداز; Classic-infantile Pompe disease; Acid alpha-glucosidase; Enzyme replacement therapy (ERT); Hypertrophic cardiomyopathy; Tachyarrhythmia;