Literature DB >> 9060103

Hand anomalies in Crouzon syndrome.

P J Anderson1, C M Hall, R D Evans, B M Jones, R D Hayward.   

Abstract

OBJECTIVE: To review the hand radiographs of patients with Crouzon syndrome, to look for extracranial manifestations of the condition at this site.
DESIGN: The hand radiographs of those with Crouzon syndrome attending the Craniofacial Service at Great Ormond Street between 1985 and 1996 were reviewed.
RESULTS: Thirty-three patients underwent a total of 34 radiographs, one patient having had a serial study. This revealed a range of minor anomalies. Most striking was the presence of carpal fusions in four cases, a feature which has not previously been reported.
CONCLUSION: The hands of Crouzon syndrome may have anomalies including carpal fusions, and these results are evidence that the condition may produce subtle effects on the hands.

Entities:  

Mesh:

Year:  1997        PMID: 9060103     DOI: 10.1007/s002560050203

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  4 in total

Review 1.  Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism.

Authors:  Nneamaka B Agochukwu; Benjamin D Solomon; Laurel J Benson; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2013-02-01       Impact factor: 2.802

Review 2.  Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses.

Authors:  Nneamaka B Agochukwu; Benjamin D Solomon; Maximilian Muenke
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

Review 3.  Revisiting Crouzon syndrome: reviewing the background and management of a multifaceted disease.

Authors:  Samuel N Helman; Arvind Badhey; Sameep Kadakia; Eugene Myers
Journal:  Oral Maxillofac Surg       Date:  2014-09-24

4.  Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.

Authors:  Meina Lin; Yongping Lu; Yu Sui; Ning Zhao; Ying Jin; Dongxu Yi; Miao Jiang
Journal:  Mol Genet Genomic Med       Date:  2019-07-18       Impact factor: 2.183

  4 in total

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