Commentary on gait analysis in Duchenne muscular dystrophy: integrating contracture, strength, and kinematic perspectives

Daniel Scherman

Rare Disease and Orphan Drugs Journal ›› 2026, Vol. 5 ›› Issue (1) -9.

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Rare Disease and Orphan Drugs Journal ›› 2026, Vol. 5 ›› Issue (1) -9. DOI: 10.20517/rdodj.2025.58
Commentary
Commentary on gait analysis in Duchenne muscular dystrophy: integrating contracture, strength, and kinematic perspectives
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Abstract

Walking ability in Duchenne muscular dystrophy (DMD) deteriorates progressively until complete loss of function. Interventions aimed at maintaining ambulatory ability rely on accurate clinical-based scores and evaluations of walking. The commentary concerns a study that provides a comprehensive look at how contractures, muscle weakness, and gait deviations intertwine to shape mobility in boys with DMD. The described eight-year longitudinal work offers a significant contribution to the understanding of longitudinal gait changes in DMD and the clinical value of such longitudinal data. The findings confirm that gait spatiotemporal parameters, particularly speed, stride length, and cadence, serve as sensitive markers of disease progression, closely linked to specific biomechanical impairments. The study strongly suggests that the integration of quantitative gait metrics into both clinical and research frameworks will be essential for optimizing patient monitoring and evaluating emerging therapeutics.

Keywords

Duchenne muscular dystrophy / gait analysis / contractures / muscle weakness / spatiotemporal parameters / pelvic kinematics

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Daniel Scherman. Commentary on gait analysis in Duchenne muscular dystrophy: integrating contracture, strength, and kinematic perspectives. Rare Disease and Orphan Drugs Journal, 2026, 5(1): -9 DOI:10.20517/rdodj.2025.58

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