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Updated: Jun 17, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
[Care continuity for patients with myopathy during transition of childhood to adulthood]
Mieko Yoshioka1, Masahiro Tsuji, Michi Kawamoto
1Department of Pediatric Neurology, Kobe City Pediatric and General Rehabilitation Center for the Challenged.
Abstract:
Recently, patients with myopathies who had not previously been able to survive after adolescence required long-term follow-up and treatment. We here discussed medical practice after adolescence in child neurology for these patients with myopathies, such as muscular dystrophies, Pompe disease and juvenile dermatomyositis. Major issues encountered in such practice included inpatient facilities and community medical networks, especially for patients who receive long-term home mechanical ventilation, management for cardiomyopathy and/or gastrogavage. A full information transfer system between child specialists and adult specialists is needed for the benefit of maturing patients.
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