Journal article
Symmetry of foot alignment and ankle flexibility in paediatric Charcot–Marie–Tooth disease
Clinical biomechanics (Bristol), Vol.27(7), pp.744-747
08/2012
DOI: 10.1016/j.clinbiomech.2012.02.006
PMCID: PMC3389135
PMID: 22424781
Abstract
Charcot–Marie–Tooth disease is the most common inherited nerve disorder and typically presents with pes cavus foot deformity and ankle equinus during childhood. Level in the variation of symmetry of musculoskeletal lower limb involvement across the clinical population is unknown, despite early reports describing gross asymmetry.
We measured foot alignment and ankle flexibility of the left and right limbs using accurate and reliable standardised paediatric outcome measures in 172 patients aged 3–20years with a variety of disease subtypes recruited from the United States, United Kingdom, Italy and Australia.
While a large range of differences existed between left and right feet for a small proportion of children, there was no overall significant difference between limbs.
There are two important implications of these findings. Children with Charcot–Marie–Tooth disease generally exhibit symmetrical foot alignment and ankle flexibility between limbs. As such, analysing one limb only for biomechanical-related research is appropriate and satisfies the independence requirements for statistical analysis. However, because there are large differences between feet for a small proportion of children, an individualised limb-focused approach to clinical care is required.
Details
- Title: Subtitle
- Symmetry of foot alignment and ankle flexibility in paediatric Charcot–Marie–Tooth disease
- Creators
- Joshua Burns - The Children's Hospital at Westmead, Sydney, NSW, AustraliaRobert Ouvrier - The Children's Hospital at Westmead, Sydney, NSW, AustraliaTim Estilow - Neuromuscular Program, The Children's Hospital of Philadelphia, PA, USARosemary Shy - Department of Pediatrics, The Children's Hospital of Michigan, Detroit, MI, USAMatilde Laurá - MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London, UKKate Eichinger - University of Rochester, Rochester, NY, USAFrancesco Muntoni - UCL Institute of Child Health, London, UKMary M Reilly - MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London, UKDavide Pareyson - IRCCS Foundation, Carlo Besta Neurological Institute, Milan, ItalyGyula Acsadi - Neurology Division, Connecticut Children's Medical Center, Hartford, CT, USAMichael E Shy - School of Medicine, Wayne State University, Detroit, MI, USARichard S Finkel - Neuromuscular Program, The Children's Hospital of Philadelphia, PA, USA
- Resource Type
- Journal article
- Publication Details
- Clinical biomechanics (Bristol), Vol.27(7), pp.744-747
- DOI
- 10.1016/j.clinbiomech.2012.02.006
- PMID
- 22424781
- PMCID
- PMC3389135
- NLM abbreviation
- Clin Biomech (Bristol)
- ISSN
- 0268-0033
- eISSN
- 1879-1271
- Publisher
- Elsevier Ltd
- Language
- English
- Date published
- 08/2012
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Stead Family Department of Pediatrics; Iowa Neuroscience Institute
- Record Identifier
- 9984020613402771
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