Population
32 patients with muscular dystrophy: 22 with LGMD2A, 5 with LGMD2I, and 5 with Becker muscular dystrophy.
Design
Cross-sectional
Authors
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Hypothesis-generating for calpain-3-specific regeneration defects in LGMD2A; prospective studies needed before clinical or therapeutic implications.
Complete lack of functional calpain 3 in LGMD2A leads to diminished muscle regeneration and aberrant regeneration signs compared to other muscular dystrophies.
Hauerslev et al. (2012) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: