Literature DB >> 16638451

Evaluation and treatment of hip dysplasia in Charcot-Marie-Tooth disease.

Gilbert Chan1, J Richard Bowen, S Jay Kumar.   

Abstract

The hip dysplasia seen in Charcot-Marie-Tooth disease is neuromuscular in nature. It usually presents in the second or third decade of life and is initially asymptomatic but may later present with pain and gait abnormalities. Treatment should be aimed at addressing the acetabular and femoral components of the dysplasia. Early recognition is essential to avoid serious morbidity associated with the condition.

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Year:  2006        PMID: 16638451     DOI: 10.1016/j.ocl.2005.12.002

Source DB:  PubMed          Journal:  Orthop Clin North Am        ISSN: 0030-5898            Impact factor:   2.472


  3 in total

Review 1.  [Hip replacement in patients with neuromuscular disorders].

Authors:  L Renner; V Drwal; F Boettner
Journal:  Orthopade       Date:  2015-07       Impact factor: 1.087

2.  Hip dysplasia is more severe in Charcot-Marie-Tooth disease than in developmental dysplasia of the hip.

Authors:  Eduardo N Novais; Sara D Bixby; John Rennick; Patrick M Carry; Young-Jo Kim; Michael B Millis
Journal:  Clin Orthop Relat Res       Date:  2014-02       Impact factor: 4.176

3.  Hip dysplasia associated with a hereditary sensorimotor polyneuropathy mimics a myopathic process.

Authors:  Mohammad Javad Hadianfard; Alireza Ashraf
Journal:  Ann Indian Acad Neurol       Date:  2012-07       Impact factor: 1.383

  3 in total

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