Literature DB >> 1739048

Klippel-Feil syndrome.

W Z McBride1.   

Abstract

The triad of short neck, low posterior hairline and severe restriction of cervical motion is a classic definition of Klippel-Feil syndrome. The anatomic and clinical expressions of this syndrome vary widely, ranging from mild cosmetic deformity to severe disability. The diagnosis is usually apparent on lateral cervical radiographs.

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Year:  1992        PMID: 1739048

Source DB:  PubMed          Journal:  Am Fam Physician        ISSN: 0002-838X            Impact factor:   3.292


  4 in total

1.  Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.

Authors:  Jawahir Y Mohamed; Eissa Faqeih; Abdulmonem Alsiddiky; Muneera J Alshammari; Niema A Ibrahim; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2013-01-03       Impact factor: 11.025

2.  Familial Klippel-Feil syndrome and paracentric inversion inv(8)(q22.2q23.3).

Authors:  R A Clarke; S Singh; H McKenzie; J H Kearsley; M Y Yip
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

3.  Sprengel deformity and Klippel-Feil syndrome leading to cervical myelopathy presentation in old age.

Authors:  Seyyed Ahmad Mirhosseini; Seyyed Mohammad Mahdy Mirhosseini; Reza Bidaki; Ahmad Pourrashidi Boshrabadi
Journal:  J Res Med Sci       Date:  2013-06       Impact factor: 1.852

4.  Prevalence of Klippel-Feil Syndrome in a Surgical Series of Patients with Cervical Spondylotic Myelopathy: Analysis of the Prospective, Multicenter AOSpine North America Study.

Authors:  Aria Nouri; Lindsay Tetreault; Juan J Zamorano; Chandan B Mohanty; Michael G Fehlings
Journal:  Global Spine J       Date:  2015-03-05
  4 in total

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