“…Atypical patients who showed LGMD -Limb girdle muscular dystrophy, DACM -Distal anterior compartment myopathy. *Novel mutation, † Mutation is predicted as nonpathogenic using UMD predictor, ‡ Bioinformatics analyses predict no deleterious effect of the mutation, Gardner-Medwin and Walton scales: grade 0 -subclinical, hyperCKemia, and tolerance of normal activities, grade 1 -normal gait, unable to run freely, grade 2 -abnormal gait, grade 3 -muscle weakness, climbing stairs with support, grade 4 -positive Gower sign, grade 5 -unable to rise from floor, grade 6 -unable to climb stairs, grade 7 -unable to get up from chairs, grade 8 -unable to walk independently, grade 9 -unable to eat, drink, or sit without support, Disease progression was evaluated using three grades: S -slow progression, only 1 grade change during the past 5 years, M -moderate progression, 2 grade changes during the past 5 years R -rapid progression, 3 or more grade changes during the past 5 years exercise intolerance or asymptomatic hyper CPKemia without muscle weakness were reported before, [3,13,14] and they may be misdiagnosed as metabolic myopathy. However, the CPK level was constantly very high in patients with dysferlinopathies, while it was fluctuating in patients with metabolic myopathies.…”