Gait and Sit-To-Stand Motor Compensation Strategies in Children and Adolescents With Duchenne Muscular Dystrophy

Author:

Dazzi Mariana De Abreu Rays1,Sá Cristina Dos Santos Cardoso De2ORCID

Affiliation:

1. Fisioterapeuta, Mestre em Ciências Pela Universidade Federal de São Paulo, São Paulo, Brazil

2. Doutora do Curso de Fisioterapia, Departamento de Ciências do Movimento Humano, Universidade Federal de São Paulo, São Paulo, Brazil

Abstract

Duchenne Muscular Dystrophy (DMD), the most common form of muscular dystrophies, is characterized by progressive and generalized muscle weakness. The weakness of the trunk and other muscle groups leads these patients to perform motor compensation strategies to maintain their lower limb functionality for gait quality and for tasks such as getting up from a sitting position. In this cross-sectional observational study, we described and quantified trunk, gait, and sit-to-stand motor compensation strategies in different stages of this disease. Thirty-one ambulatory 5–18-year-old children and adolescents with a diagnosis of DMD, underwent cognitive assessment with the Mental Mini-Examination (MMSE) and motor assessment with the Vignos scale, Segmental Assessment of Trunk Control (SATCo-BR), Timed Up and Go test (TUG Test), and 10-m walk test. We found strong correlations between trunk and gait compensations, and identified motor compensation strategies characteristic of certain DMD classifications. Also, these lower limb and trunk compensations related to disease staging (Vignos) such that compensations were fewer for patients at relatively better disease staging.

Publisher

SAGE Publications

Subject

Sensory Systems,Experimental and Cognitive Psychology

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