Current concepts review: Orthopaedic aspects of Charcot-Marie-Tooth disease

Foot and Ankle International

Volumn 27, Issue 11, 2006, Pages 1003-1010

  Guyton, Gregory P ^a,b  

^a Union Memorial Hospital ^*

^b UNION MEMORIAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; ARTHRODESIS; CONSERVATIVE TREATMENT; DIAGNOSTIC IMAGING; DISEASE CLASSIFICATION; FOOT MALFORMATION; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; LIMB WEAKNESS; ORTHOPEDIC SURGERY; OSTEOTOMY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; REVIEW;

EID: 33750564961     PISSN: 10711007     EISSN: None     Source Type: Journal    
DOI: 10.1177/107110070602701125     Document Type: Review

References (32)

1. Alexander, IJ; Johnson, KA: Assessment and management of pes cavus in Charcot-Marie-tooth disease. Clin. Orthop. 246:273-281, 1989.
2. Berciano, J; Garcia, A; Calleja, J; Combarros, O: Clinico- electrophysiological correlation of extensor digitoram brevis muscle atrophy in children with Charcot-Marie-Tooth disease 1A duplication. Neuromuscul. Disord. 10:419-424, 2000.
3. Berciano, J; Garcia, A; Combarros, O: Initial semeiology in children with Charcot-Marie-Tooth disease 1A duplication. Muscle Nerve. 27:34-39, 2003.
4. Brewerton, DA; Sandifer, PH; Sweetnam, DR: "Idiopathic" pes cavus; an investigation into its aetiology. Br. Med J. 2:659-661, 1963.
5. Charcot, JM; Marie, P: Sur une forme particulière d'atrophie musculaire progressive, souvent familiale débutant par les pieds et les jambes et atteignant plus tard les mains. Revue Med. Paris 6:97-138, 1886.
6. Dyck, PJ; Chance, P; Lebo, R; Carney, JA: Hereditary motor and sensory neuropathies. In: Dyck, PJ; Thomas, PK; Griffin, JW; Low, PA; Poduslo, JF (eds.) Peripheral neuropathy. 3rd ed. W.B. Saunders, Philadelphia, pp. 1094-1136, 1993.
7. Dyck, PJ; Lais, AC; Offord, KP: The nature of myelinated nerve fiber degeneration in dominantly inherited hypertrophic neuropathy. Mayo Clin. Proc. 49:34-39, 1974.
8. Dwyer, FC: Osteotomy of the calcaneum for pes cavus. J. Bone Joint Surg. 41-B:80-86, 1959.
9. Gallardo, E; Garcia, A; Combarros, O; Berciano, J: Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles. Brain. 129(Pt 2):426-437, 2006.
10. Guyton, GP: Peroneal nerve branching suggests compression palsy in the deformities of CMT. Clin. Orthop. 2006 in press.
11. Guyton, GP; Mann, RA: The pathogenesis and surgical management of foot deformity in Charcot-Marie-Tooth disease. Foot Ankle Clin. 5:317-326, 2000.
12. Holmes, JR; Hansen, ST: Foot and ankle manifestations of Charcot-Marie-Tooth disease. Foot Ankle 14:476-486, 1993.
13. Jafarnia, K; Sullivan, MJ; Hildreth, DH: Hereditary neuropathy with liability to pressure palsies: a case report. Clin. Orthop. 385:253-255, 2001.
14. Jones, R: An operation for paralytic calcaneocavus. Am. J. Orthop. Surg. 5:371, 1908.
15. Mann, DC; Hsu, JD: Triple arthrodesis in the treatment of fixed cavovarus deformity in adolescent patients with Charcot-Marie-Tooth disease. Foot Ankle. 13:1-6, 1992.
16. Mann, RA; Missirian, J: Pathophysiology of Charcot-Marie-Tooth disease. Clin. Orthop. 234:221-228, 1988.
17. Mariman, EC; Gabreels-Festen, AA; van Beersum, SE; et al.: Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies. Ann. Neurol. 36:650-655, 1994.
18. Nagai, MK; Chan, G; Guille, JT; et al.: Prevalence of Charcot-Marie-Tooth disease in patients who have bilateral cavovarus feet. J. Pediatr. Orthop. 26:438-443, 2006.
19. Niemann, A; Berger, P; Suter, U: Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease. Neuromolecular Med. 8:217-242, 2006.
20. Paulos, L; Coleman, SS; Samuelson, KM: Pes cavovarus. Review of a surgical approach using selective soft-tissue procedures. J. Bone Joint Surg. 62-A:942-953, 1980.
21. Reilly, MM; Hanna, MG: Genetic neuromuscular disease. J. Neurol. Neurosurg. Psychiatry 73 (Suppl 2):12-21, 2002.
22. Roper, BA; Tibrewal, SB: Soft tissue surgery in Charcot-Marie-Tooth disease. J. Bone Joint Surg. 71-B:17-20, 1989.
23. Sabir, M; Lyttle, D: Pathogenesis of pes cavus in Charcot-Marie-Tooth disease. Clin. Orthop. 175:173-178, 1983.
24. Samilson, RL: Crescentic osteotomy of the os calcis for calcaneocavus feet. In Bateman, JR (ed.), Foot science, Saunders, Philadelphia, 1976.
25. Santavirta, S; Turunen, V; Ylinen, P; Konttinen, YT; Tallroth, K: Foot and ankle fusions in Charcot-Marie-Tooth disease. Arch. Orthop. Trauma Surg. 112:175-179, 1993.
26. Siffert, RS; delTorto, U: "Beak" triple arthrodesis for severe cavus deformity. Clin. Orthop. 181:64-67, 1983.
27. Steindler, A: Operative treatment of pes cavus: stripping of the os calcis. Surg. Oynecol. Obstet. 24:612, 1917.
28. Tooth, HH: The peroneal type of progressive muscular atrophy. Cambridge University Dissertation, H. K. Lewis, London, 1886.
29. Tynan, MC; Klenerman, L; Helliwell, TR; Edwards, RH; Hayward, M. Investigation of muscle imbalance in the leg in symptomatic forefoot pes cavus: a multidisciplinary study. Foot Ankle 13:489-501, 1992.
30. Tynan, MC; Klenerman, L: The modified Robert Jones tendon transfer in cases of pes cavus and clawed hallux. Foot Ankle Int. 15:68-71, 1994.
31. Wetmore, RS; Drennan, JC: Long-term results of triple arthrodesis in Charcot-Marie-Tooth disease. J. Bone Joint Surg. 71-A:417-422, 1989.
32. Wukich, DK; Bowen, JR: A long-term study of triple arthrodesis for correction of pes cavovarus in Charcot-Marie-Tooth disease. J. Pediatr Orthop. 9:433-437, 1989.