Abstract
Background
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.
Methods
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
3–20 years with a variety of disease subtypes recruited from the United States, United
Kingdom, Italy and Australia.
Findings
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.
Interpretation
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.
Keywords
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References
- Comparison of CMT1A and CMT2: similarities and differences.J. Neurol. 2006; 253: 1572-1580
- Weight bearing ankle dorsiflexion range of motion in idiopathic pes cavus compared to normal and pes planus feet.Foot. 2005; 15: 91-94
- The effect of pes cavus on foot pain and plantar pressure.Clin. Biomech. 2005; 20: 877-882
- Ascorbic acid for Charcot–Marie–Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trial.Lancet Neurol. 2009; 8: 537-544
- Validation of the CMT Pediatric Scale as an outcome measure of disability.Ann. Neurol. 2012; (Electronic publication ahead of print)https://doi.org/10.1002/ana.23572
- Foot morphology and foot/ankle injury in indoor football.J. Sci. Med. Sport. 2007; 10: 311-319
- Sur une forme particulière d'atrophie musculaire progressive, souvent familiale débutant par les pieds et les jambes et atteignant plus tard les mains.Rev. Med. (Paris). 1886; 6: 97-138
- Clinical variability in two pairs of identical twins with the Charcot–Marie–Tooth disease type 1A duplication.Neurology. 1995; 45: 2090-2093
- The Foot Posture Index: Rasch analysis of a novel, foot-specific outcome measure.Arch. Phys. Med. Rehabil. 2007; 88: 88-93
- Hip and ankle range of motion in elite classical ballet dancers and controls.Clin. J. Sport Med. 1997; 7: 174-179
- Analysis of paired data in physical therapy research: time to stop double dipping?.J. Orthop. Sports Phys. Ther. 2005; 35: 477-478
- Validity of 3 clinical techniques for the measurement of static foot posture in older people.J. Orthop. Sports Phys. Ther. 2005; 35: 479-486
- Development and validation of a novel rating system for scoring standing foot posture: the foot posture index.Clin. Biomech. 2006; 21: 89-98
- Normative values for the Foot Posture Index.J. Foot Ankle Res. 2008; 1: 6
- Genetic and clinical aspects of Charcot–Marie–Tooth disease.Clin. Genet. 1974; 6: 98-118
- Foot deformities in children with hereditary motor and sensory neuropathy.J. Pediatr. Orthop. 2005; 25: 241-244
Article info
Publication history
Published online: March 19, 2012
Accepted:
February 16,
2012
Received:
December 7,
2011
Identification
Copyright
© 2012 Elsevier Ltd. Published by Elsevier Inc. All rights reserved.