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Volumn 37, Issue 2, 2006, Pages 203-209

Evaluation and Treatment of Hip Dysplasia in Charcot-Marie-Tooth Disease

Author keywords

[No Author keywords available]

Indexed keywords

CALLUS; COMPUTER ASSISTED TOMOGRAPHY; DISEASE SEVERITY; DNA DETERMINATION; ELECTROPHYSIOLOGY; EVOKED MUSCLE RESPONSE; EVOKED SOMATOSENSORY RESPONSE; FEMUR; HEREDITARY MOTOR SENSORY NEUROPATHY; HIP DYSPLASIA; HIP OSTEOTOMY; HUMAN; NERVE BIOPSY; NERVE PARALYSIS; PATIENT MONITORING; PHYSIOTHERAPY; POSTOPERATIVE COMPLICATION; PRIORITY JOURNAL; REVIEW; SCIATIC NERVE; SUBLUXATION; SURAL NERVE; SURGICAL TECHNIQUE;

EID: 33646086725     PISSN: 00305898     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ocl.2005.12.002     Document Type: Review
Times cited : (21)

References (27)
  • 1
    • 0016266593 scopus 로고
    • Genetic and clinical aspects of Charcot-Marie-Tooth's disease
    • Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth's disease. Clin Genet 6 2 (1974) 98-118
    • (1974) Clin Genet , vol.6 , Issue.2 , pp. 98-118
    • Skre, H.1
  • 2
    • 0025998134 scopus 로고
    • Population frequencies of inherited neuromuscular diseases-a world survey
    • Emery A.E. Population frequencies of inherited neuromuscular diseases-a world survey. Neuromuscul Disord 1 1 (1991) 19-29
    • (1991) Neuromuscul Disord , vol.1 , Issue.1 , pp. 19-29
    • Emery, A.E.1
  • 3
    • 0026849499 scopus 로고
    • Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
    • Lupski J.R., Wise C.A., Kuwano A., et al. Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A. Nat Genet 1 1 (1992) 29-33
    • (1992) Nat Genet , vol.1 , Issue.1 , pp. 29-33
    • Lupski, J.R.1    Wise, C.A.2    Kuwano, A.3
  • 4
    • 0014301249 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies
    • Dyck P.J., and Lambert E.H. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies. Arch Neurol 18 6 (1968) 603-618
    • (1968) Arch Neurol , vol.18 , Issue.6 , pp. 603-618
    • Dyck, P.J.1    Lambert, E.H.2
  • 5
    • 0141864610 scopus 로고    scopus 로고
    • Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies
    • Saifi G.M., Szigeti K., Snipes G.J., et al. Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies. J Investig Med 51 5 (2003) 261-283
    • (2003) J Investig Med , vol.51 , Issue.5 , pp. 261-283
    • Saifi, G.M.1    Szigeti, K.2    Snipes, G.J.3
  • 6
    • 0027108731 scopus 로고
    • De-novo mutation in hereditary motor and sensory neuropathy type I
    • Hoogendijk J.E., Hensels G.W., Gabreels-Festen A.A., et al. De-novo mutation in hereditary motor and sensory neuropathy type I. Lancet 339 8801 (1992) 1081-1082
    • (1992) Lancet , vol.339 , Issue.8801 , pp. 1081-1082
    • Hoogendijk, J.E.1    Hensels, G.W.2    Gabreels-Festen, A.A.3
  • 7
    • 0029863589 scopus 로고    scopus 로고
    • Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
    • Nelis E., Van Broeckhoven C., De Jonghe P., et al. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study. Eur J Hum Genet 4 1 (1996) 25-33
    • (1996) Eur J Hum Genet , vol.4 , Issue.1 , pp. 25-33
    • Nelis, E.1    Van Broeckhoven, C.2    De Jonghe, P.3
  • 8
    • 0027374931 scopus 로고
    • Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication
    • Wise C.A., Garcia C.A., Davis S.N., et al. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. Am J Hum Genet 53 4 (1993) 853-863
    • (1993) Am J Hum Genet , vol.53 , Issue.4 , pp. 853-863
    • Wise, C.A.1    Garcia, C.A.2    Davis, S.N.3
  • 9
    • 0023722767 scopus 로고
    • Pathophysiology of Charcot-Marie-Tooth disease
    • Mann R.A., and Missirian J. Pathophysiology of Charcot-Marie-Tooth disease. Clin Orthop 234 (1988) 221-228
    • (1988) Clin Orthop , vol.234 , pp. 221-228
    • Mann, R.A.1    Missirian, J.2
  • 10
    • 0020585474 scopus 로고
    • Pathogenesis of pes cavus in Charcot-Marie-Tooth disease
    • Sabir M., and Lyttle D. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease. Clin Orthop 175 (1983) 173-178
    • (1983) Clin Orthop , vol.175 , pp. 173-178
    • Sabir, M.1    Lyttle, D.2
  • 11
    • 0021138932 scopus 로고
    • Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship
    • Sabir M., and Lyttle D. Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship. Clin Orthop 184 (1984) 223-235
    • (1984) Clin Orthop , vol.184 , pp. 223-235
    • Sabir, M.1    Lyttle, D.2
  • 12
    • 0022632526 scopus 로고
    • Spinal deformities in patients with Charcot-Marie-tooth disease. A review of 12 patients
    • Daher Y.H., Lonstein J.E., Winter R.B., et al. Spinal deformities in patients with Charcot-Marie-tooth disease. A review of 12 patients. Clin Orthop 202 (1986) 219-222
    • (1986) Clin Orthop , vol.202 , pp. 219-222
    • Daher, Y.H.1    Lonstein, J.E.2    Winter, R.B.3
  • 13
    • 0017275503 scopus 로고
    • Spinal deformity associated with heritable neurological conditions: spinal muscular atrophy, Friedreich's ataxia, familial dysautonomia, and Charcot-Marie-Tooth disease
    • Hensinger R.N., and MacEwen G.D. Spinal deformity associated with heritable neurological conditions: spinal muscular atrophy, Friedreich's ataxia, familial dysautonomia, and Charcot-Marie-Tooth disease. J Bone Joint Surg Am 58 1 (1976) 13-24
    • (1976) J Bone Joint Surg Am , vol.58 , Issue.1 , pp. 13-24
    • Hensinger, R.N.1    MacEwen, G.D.2
  • 14
    • 0021854654 scopus 로고
    • Hip dysplasia associated with Charcot-Marie-Tooth disease in the older child and adolescent
    • Kumar S.J., Marks H.G., Bowen J.R., et al. Hip dysplasia associated with Charcot-Marie-Tooth disease in the older child and adolescent. J Pediatr Orthop 5 5 (1985) 511-514
    • (1985) J Pediatr Orthop , vol.5 , Issue.5 , pp. 511-514
    • Kumar, S.J.1    Marks, H.G.2    Bowen, J.R.3
  • 15
    • 0030167281 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease associated with hip dysplasia: a case report
    • Cucuzzella T.R., Guille J.T., and MacEwen G.D. Charcot-Marie-Tooth disease associated with hip dysplasia: a case report. Del Med J 68 6 (1996) 305-307
    • (1996) Del Med J , vol.68 , Issue.6 , pp. 305-307
    • Cucuzzella, T.R.1    Guille, J.T.2    MacEwen, G.D.3
  • 16
    • 0029042230 scopus 로고
    • Acetabular dysplasia and Charcot-Marie-Tooth disease in a family. A report of four cases
    • Fuller J.E., and DeLuca P.A. Acetabular dysplasia and Charcot-Marie-Tooth disease in a family. A report of four cases. J Bone Joint Surg Am 77 7 (1995) 1087-1091
    • (1995) J Bone Joint Surg Am , vol.77 , Issue.7 , pp. 1087-1091
    • Fuller, J.E.1    DeLuca, P.A.2
  • 17
    • 0036210785 scopus 로고    scopus 로고
    • The association between Charcot-Marie-Tooth disease and developmental dysplasia of the hip
    • McGann R., and Gurd A. The association between Charcot-Marie-Tooth disease and developmental dysplasia of the hip. Orthopedics 25 3 (2002) 337-339
    • (2002) Orthopedics , vol.25 , Issue.3 , pp. 337-339
    • McGann, R.1    Gurd, A.2
  • 18
    • 0026647816 scopus 로고
    • Hip dysplasia in hereditary motor and sensory neuropathies
    • Pailthorpe C.A., and Benson M.K. Hip dysplasia in hereditary motor and sensory neuropathies. J Bone Joint Surg Br 74 4 (1992) 538-540
    • (1992) J Bone Joint Surg Br , vol.74 , Issue.4 , pp. 538-540
    • Pailthorpe, C.A.1    Benson, M.K.2
  • 19
    • 0042012958 scopus 로고    scopus 로고
    • Hip dysplasia in Charcot-Marie-Tooth disease: report of a family
    • Ushiyama T., Tanaka C., Kawasaski T., et al. Hip dysplasia in Charcot-Marie-Tooth disease: report of a family. J Orthop Sci 8 4 (2003) 610-612
    • (2003) J Orthop Sci , vol.8 , Issue.4 , pp. 610-612
    • Ushiyama, T.1    Tanaka, C.2    Kawasaski, T.3
  • 20
    • 0032907068 scopus 로고    scopus 로고
    • Developmental hip dysplasia in hereditary motor and sensory neuropathy type 1
    • van Erve R.H., and Driessen A.P. Developmental hip dysplasia in hereditary motor and sensory neuropathy type 1. J Pediatr Orthop 19 1 (1999) 92-96
    • (1999) J Pediatr Orthop , vol.19 , Issue.1 , pp. 92-96
    • van Erve, R.H.1    Driessen, A.P.2
  • 21
    • 0028115887 scopus 로고
    • Hip abnormalities in children with Charcot-Marie-Tooth disease
    • Walker J.L., Nelson K.R., Heavilon J.A., et al. Hip abnormalities in children with Charcot-Marie-Tooth disease. J Pediatr Orthop 14 1 (1994) 54-59
    • (1994) J Pediatr Orthop , vol.14 , Issue.1 , pp. 54-59
    • Walker, J.L.1    Nelson, K.R.2    Heavilon, J.A.3
  • 22
    • 0037641073 scopus 로고    scopus 로고
    • Prevention of damage caused by sural nerve withdrawal for nerve grafting
    • Brunelli G.A. Prevention of damage caused by sural nerve withdrawal for nerve grafting. Hand Surg 7 2 (2002) 163-166
    • (2002) Hand Surg , vol.7 , Issue.2 , pp. 163-166
    • Brunelli, G.A.1
  • 24
    • 12144286544 scopus 로고    scopus 로고
    • Microsurgical repair of the sural nerve after nerve biopsy to avoid associated sensory morbidity: a preliminary report
    • [discussion 900-1]
    • Schoeller T., Huemer G.M., Shafighi M., et al. Microsurgical repair of the sural nerve after nerve biopsy to avoid associated sensory morbidity: a preliminary report. Neurosurgery 54 4 (2004) 897-900 [discussion 900-1]
    • (2004) Neurosurgery , vol.54 , Issue.4 , pp. 897-900
    • Schoeller, T.1    Huemer, G.M.2    Shafighi, M.3
  • 25
    • 0032994144 scopus 로고    scopus 로고
    • The periacetabular osteotomy. Minimum 2 year followup in more than 100 hips
    • Trumble S.J., Mayo K.A., and Mast J.W. The periacetabular osteotomy. Minimum 2 year followup in more than 100 hips. Clin Orthop 363 (1999) 54-63
    • (1999) Clin Orthop , vol.363 , pp. 54-63
    • Trumble, S.J.1    Mayo, K.A.2    Mast, J.W.3
  • 26
    • 0031009153 scopus 로고    scopus 로고
    • Dynamics of hip joint remodeling after Chiari osteotomy. 10 patients with neuromuscular disease followed for 8 years
    • Osebold W.R., Lester E.L., and Watson P. Dynamics of hip joint remodeling after Chiari osteotomy. 10 patients with neuromuscular disease followed for 8 years. Acta Orthop Scand 68 2 (1997) 128-132
    • (1997) Acta Orthop Scand , vol.68 , Issue.2 , pp. 128-132
    • Osebold, W.R.1    Lester, E.L.2    Watson, P.3
  • 27
    • 18144418224 scopus 로고    scopus 로고
    • A new modified technique of triple osteotomy of the innominate bone for acetabular dysplasia
    • Lipton G.E., and Bowen J.R. A new modified technique of triple osteotomy of the innominate bone for acetabular dysplasia. Clin Orthop 434 (2005) 78-85
    • (2005) Clin Orthop , vol.434 , pp. 78-85
    • Lipton, G.E.1    Bowen, J.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.