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Title
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Gait abnormalities in people with Dravet syndrome : a cross-sectional multi-center study
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Author
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Abstract
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| Objective To quantify gait abnormalities in people with Dravet syndrome (DS). Methods Individuals with a confirmed diagnosis of DS were enrolled, and stratified according to knee flexion at initial contact (IC) and range of motion (ROM) during stance (atypical crouch: knee flexion >20° at IC and knee ROM >15° during stance; straight: knee flexion <20° at IC). A 1D ANOVA (α = 0.05) was used to test statistical differences among the joint kinematics and spatio–temporal parameters of the cohort and an age-matched control group. Clinical (neurological and orthopaedic evaluation) and anamnestic data (seizure type, drugs, genetic mutation) were collected; distribution between the two gait phenotypes was assessed with the Fisher exact test and, for mutation, with the chi-squared test (p < 0.05). Linear regression between maximum knee flexion and normalised walking speed was calculated. Results Seventy-one subjects were enrolled and evaluated with instrumented gait analysis. Fifty-two were included in final analysis (mean age 13.8 ± 7.3; M 26). Two gait patterns were detected: an atypical crouch gait (34.6%) with increased ankle, knee and hip flexion during stance, and reduced walking speed and stride length not associated with muscle-tendon retractions; and a pattern resembling those of healthy age-matched controls, but still showing reduced walking speed and stride length. No differences in clinical or anamnestic data emerged between the two groups. Significance Objectively quantified gait in DS shows two gait patterns with no clear-cut relation to clinical data. Kinematics abnormalities may be related to stabilization issues. These findings may guide rehabilitative and preventive measures. |
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Language
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English
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Source (journal)
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European journal of paediatric neurology. - London
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Publication
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London
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2019
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ISSN
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1090-3798
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DOI
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10.1016/J.EJPN.2019.09.010
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Volume/pages
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23
:6
(2019)
, p. 808-818
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ISI
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000501655400008
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Pubmed ID
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31582194
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Full text (Publisher's DOI)
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Full text (open access)
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Full text (publisher's version - intranet only)
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