Glycogen storage disease type II, also known as Pompe disease, is a rare, progressive disorder. It is characterized by partial or total deficiency of acid alpha-glucosidase (GAA), an enzyme that hydrolyzes lysosomal glycogen [1]. As a result of deficiency of GAA enzyme, lysosomal glycogen accumulates in tissues of the body, which can lead to progressive debilitation, organ failure, and death. The diagnosis of Pompe disease in children and adults can be challenging because of the heterogeneous clinical presentation and considerable overlap of signs and symptoms identified in other neuromuscular diseases [1]. The infantile-onset form of the disease is rapidly progressive which is characterized by marked cardiomyopathy, respiratory failure, and death within the first year of life [2]. Late-onset Pompe disease can present from the age of 1 year to the sixth decade of life which is characterized by progressive proximal skeletal muscle weakness and respiratory insufficiency that leads to respiratory failure and death [3,4]. Enzyme replacement therapy (ERT) using recombinant human acid alpha-glucosidase was developed as the most promising therapeutic approach for Pompe disease although the clinical response is variable; however, the evidence is lacking, especially regarding the optimal dose or dose frequency and the effect of long-term alglucosidase alfa treatment on extended survival as well as ventilation-free survival and cardiomyopathy [5]. Recently, Kim et al. [6] published clinical features, genotypes, changes before and after ERT, and long-term outcomes in 5 Korean patients with infantile-onset Pompe disease (IOPD) and late-onset Pompe disease (LOPD). During a median 10-year ERT, there remains stable in the abnormalities shown on initial echocardiogram in patients with IOPD, along with improved organomegaly and normalization of liver transaminase level in patients with late-onset Pompe disease without adverse effects. Usually, clinical effectiveness in Pompe disease is evaluated by ventilator-free survival, reduction in left ventricular mass index, and improvement of motor function. The study by Kim et al. [6] was well conducted on this score to assess clinical effectiveness including quality of life in patients with Pompe disease. To evaluate the functional exercise capacity, there are several modalities available. The modality used should be chosen based on the clinical questions to be addressed and on available resources [7]. The most popular clinical exercise tests in the order of increasing complexity are stair climbing, a 6-minute walk test (6-MWT), a shuttle-walk test, a cardiac stress test (e.g., Bruce protocol), and a cardiopulmonary exercise test [8]. A recent review of functional walking tests concluded that “the 6-MWT is easy to administer, better tolerated, and more reflective of activities of daily living than the other walk tests [9]. The 6-MWT is a practical and simple test that requires a 100-ft hallway but no exercise equipment or advanced training for technicians are needed [6,7]. It assesses the global and integrated responses of all the systems involved during the exercise, including the cardiovascular and pulmonary systems, systemic and peripheral circulation, blood, neuromuscular units, and muscle metabolism [9]. However, as a 6-MWT can be evaluated only in patients capable of independent walking, Kim et al. [6] conducted a motor function measurement using manual muscle testing method to overcome these limitations in patients incapable of independent walking.