Prevalence and orthopedic management of foot and ankle deformities in Charcot–Marie–Tooth disease. Issue 2 (7th July 2017)

• Record Type: Journal Article
• Authors: Laurá, Matilde; Singh, Dishan; Ramdharry, Gita; Morrow, Jasper; Skorupinska, Mariola; Pareyson, Davide; Burns, Joshua; Lewis, Richard A.; Scherer, Steven S.; Herrmann, David N.; Cullen, Nicholas; Bradish, Christopher; Gaiani, Luca; Martinelli, Nicolò; Gibbons, Paul; Pfeffer, Glenn; Phisitkul, Phinit; Wapner, Keith; Sanders, James; Flemister, Sam; Shy, Michael E.; Reilly, Mary M.
• Is Part Of: Muscle & nerve. Volume 57:Issue 2(2018)
• Page Start: 255
• Page End: 259
• Publication Date: 2017-07-07
• Subjects: Charcot–Marie–Tooth disease -- foot deformities -- foot surgery -- orthopedic complications -- pes cavus -- survey; Neuromuscular diseases -- Periodicals; Muscles -- Periodicals; Nerves -- Periodicals; 616.74
• DOI: 10.1002/mus.25724
• Languages: English
• ISSNs: 0148-639X

Abstract

ABSTRACT: Introduction: Foot deformities are frequent complications in Charcot–Marie–Tooth disease (CMT) patients, often requiring orthopedic surgery. However, there are no prospective, randomized studies on surgical management, and there is variation in the approaches among centers both within and between countries. Methods: In this study we assessed the frequency of foot deformities and surgery among patients recruited into the Inherited Neuropathies Consortium (INC). We also designed a survey addressed to orthopedic surgeons at INC centers to determine whether surgical approaches to orthopedic complications in CMT are variable. Results: Foot deformities were reported in 71% of CMT patients; 30% of the patients had surgery. Survey questions were answered by 16 surgeons working in different specialized centers. Most of the respondents were foot and ankle surgeons. There was marked variation in surgical management. Discussion: Our findings confirm that the approaches to orthopedic management of CMT are varied. We identify areas that require further research. Muscle Nerve 57 : 255–259, 2018