Document Detail


Larsen syndrome: a review of the literature and case report.
MedLine Citation:
PMID:  21044106     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
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.
Authors:
Anand K Sajnani; Cynthia K Y Yiu; Nigel M King
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Publication Detail:
Type:  Journal Article     Date:  2010-10-19
Journal Detail:
Title:  Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry     Volume:  30     ISSN:  1754-4505     ISO Abbreviation:  Spec Care Dentist     Publication Date:    2010 Nov-Dec
Date Detail:
Created Date:  2010-11-03     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8103755     Medline TA:  Spec Care Dentist     Country:  United States    
Other Details:
Languages:  eng     Pagination:  255-60     Citation Subset:  D    
Copyright Information:
©2010 Special Care Dentistry Association and Wiley Periodicals, Inc.
Affiliation:
Terna Dental College and Hospital, Navi Mumbai, India.
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