Literature DB >> 18842446

[Camptodactyly].

B Salazard1, V Quilici, P Samson.   

Abstract

Camptodactyly is a permanent, nontraumatic flexion of the proximal interphalangeal joint. The prevalence is around 1% and the little finger is most commonly affected. Two groups may be identified, depending on the age of onset: camptodactyly severe within 2-3 years or beginning in the early teens. Many anatomical abnormalities have been incriminated as the cause of camptodactyly: anomalous lumbrical muscle, short flexor digitorum superficialis, retractile subcutaneous tissue, anomalous extensor muscle. Splinting is always required, with dynamic and/or static splinting of the proximal interphalangeal joint. If improvement is not obtained with splinting, surgery can be proposed. Surgical treatment must correct the soft tissue contracture (flap and skin graft), the tendinous anatomical abnormalities and the joint contracture. Splinting and physiotherapy is necessary after surgery.

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Year:  2008        PMID: 18842446     DOI: 10.1016/j.main.2008.07.018

Source DB:  PubMed          Journal:  Chir Main        ISSN: 1297-3203


  2 in total

1.  Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly.

Authors:  Hao Deng; Sheng Deng; Hongbo Xu; Han-Xiang Deng; Yulan Chen; Lamei Yuan; Xiong Deng; Shengbo Yang; Liping Guan; Jianguo Zhang; Hong Yuan; Yi Guo
Journal:  PLoS One       Date:  2016-05-25       Impact factor: 3.240

2.  NOSOLOGY OF HAND DISEASES IN CHILDREN AND ADOLESCENTS OPERATED IN PROVISIONAL FACILITIES IN A MODEL HOSPITAL - PERNAMBUCO STATE, BRAZIL.

Authors:  Mauri Cortez; Rui Ferreira da Silva; Alain Gilbert; Carlos Teixeira Brandt; Philippe Valenti
Journal:  Rev Bras Ortop       Date:  2015-12-12
  2 in total

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