A. Krithika

Supraventricular Tachycardia as an Unusual Presentation of Infantile Onset Pompe Disease: A Case Report

Pompe disease is a rare autosomal recessive lysosomal storage disorder with an incidence of approximately one in 40,000 live births is caused by deficiency of acid α-glucosidase, leading to progressive glycogen accumulation in cardiac and skeletal muscle. Infantile Onset Pompe Disease (IOPD) represents the most severe...