Literature DB >> 20638922

Posture and gait abilities in patients with myotonic dystrophy (Steinert disease). Evaluation on the short-term of a rehabilitation program.

B Missaoui1, E Rakotovao, S Bendaya, M Mane, B Pichon, M Faucher, P Thoumie.   

Abstract

OBJECTIVES: To evaluate the effects of a rehabilitation program in terms of balance, gait and muscle strength in a population of patients with myotonic dystrophy. PATIENTS: Twenty patients benefited, as outpatients in a hospital setting, from a rehabilitation program with clinical and instrumental evaluations. The evaluation focused on quantitative balance measurement by clinical and stabilometer tests, gait assessed by Locometre and extensors and flexors knee muscle strength measured in isokinetic concentric mode at 60°/s.
RESULTS: After the rehabilitation program, we observed a significant improvement in the patients' balance capacities measured with the Berg Balance Scale (BBS), fast gait speed and muscle strength. However, the instrumental evaluation did not report any gains for static balance and spontaneous gait speed after the training program. No correlation was found between the various improvements.
CONCLUSION: A rehabilitation program focused on strength, gait and balance allowed for significant improvements in some parameters of myotonic dystrophy. These results attest to the relevance of a short-term rehabilitation protocol for these patients in the framework of a multidisciplinary therapeutic care. The disparity observed in the results measured for these patients suggest the contribution of cognitive involvement in the limitations felt by patients with myotonic dystrophy in the areas of gait and balance. Copyright 2010 Elsevier Masson SAS. All rights reserved.

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Year:  2010        PMID: 20638922     DOI: 10.1016/j.rehab.2010.06.004

Source DB:  PubMed          Journal:  Ann Phys Rehabil Med        ISSN: 1877-0657


  4 in total

1.  Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA).

Authors:  Giovanni DiPaolo; Cecilia Jimenez-Moreno; Nikoletta Nikolenko; Antonio Atalaia; Darren G Monckton; Michela Guglieri; Hanns Lochmüller
Journal:  J Neurol       Date:  2017-02-06       Impact factor: 4.849

Review 2.  What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review.

Authors:  Marie-Pier Roussel; Marika Morin; Cynthia Gagnon; Elise Duchesne
Journal:  BMC Musculoskelet Disord       Date:  2019-03-05       Impact factor: 2.362

3.  Paving the way for a better understanding of the pathophysiology of gait impairment in myotonic dystrophy: a pilot study focusing on muscle networks.

Authors:  Antonino Naro; Simona Portaro; Demetrio Milardi; Luana Billeri; Antonino Leo; David Militi; Placido Bramanti; Rocco Salvatore Calabrò
Journal:  J Neuroeng Rehabil       Date:  2019-09-18       Impact factor: 4.262

4.  Balance impairment in myotonic dystrophy type 1: Dynamic posturography suggests the coexistence of a proprioceptive and vestibular deficit.

Authors:  Stefano Scarano; Valeria Ada Sansone; Carola Rita Ferrari Aggradi; Elena Carraro; Luigi Tesio; Maurizio Amadei; Viviana Rota; Alice Zanolini; Antonio Caronni
Journal:  Front Hum Neurosci       Date:  2022-07-28       Impact factor: 3.473

  4 in total

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