Literature DB >> 21044106

Larsen syndrome: a review of the literature and case report.

Anand K Sajnani1, Cynthia K Y Yiu, Nigel M King.   

Abstract

Larsen syndrome is a rare genetic disorder characterized by multiple dislocations of the large joints and characteristic craniofacial abnormalities. It exists in both a severe autosomal recessive form and a mild autosomal dominant variety. To date, only three authors have reported oral findings for this syndrome. This paper describes an 8-year-old Chinese boy with Larsen syndrome who had advanced periodontitis. The need for periodontal therapy and regular monitoring of such patients has been highlighted. ©2010 Special Care Dentistry Association and Wiley Periodicals, Inc.

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Year:  2010        PMID: 21044106     DOI: 10.1111/j.1754-4505.2010.00163.x

Source DB:  PubMed          Journal:  Spec Care Dentist        ISSN: 0275-1879


  2 in total

1.  A case study of atypical Larsen syndrome with absent hallmark joint dislocations.

Authors:  Neslida Kodra; Callie Diamonstein; Natalie S Hauser
Journal:  Mol Genet Genomic Med       Date:  2019-03-27       Impact factor: 2.183

2.  An orthodontic perspective on Larsen syndrome.

Authors:  Madoka Yasunaga; Hiroyuki Ishikawa; Kenichi Yanagita; Sachio Tamaoki
Journal:  BMC Oral Health       Date:  2021-03-10       Impact factor: 2.757

  2 in total

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