Document Detail


Multiple odontogenic keratocysts in mental retardation-overgrowth (Simpson-Golabi-Behmel) syndrome.
MedLine Citation:
PMID:  10864729     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We report on a 10-year-old boy with mental retardation-overgrowth (Simpson-Golabi-Behmel) syndrome. The child had the typical clinical features including, postnatal overgrowth, mental retardation, and a characteristic facial appearance. He was admitted for treatment of multiple mandibular and maxillary cysts. Histopathological examination of the cyst tissue showed keratinized epithelium. Odontogenic keratocysts may have to be added to the typical features of this syndrome.
Authors:
M Krimmel; S Reinert
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The British journal of oral & maxillofacial surgery     Volume:  38     ISSN:  0266-4356     ISO Abbreviation:  Br J Oral Maxillofac Surg     Publication Date:  2000 Jun 
Date Detail:
Created Date:  2000-08-17     Completed Date:  2000-08-17     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  8405235     Medline TA:  Br J Oral Maxillofac Surg     Country:  SCOTLAND    
Other Details:
Languages:  eng     Pagination:  221-3     Citation Subset:  D; IM    
Copyright Information:
Copyright 2000 The British Association of Oral and Maxillofacial Surgeons.
Affiliation:
Department of Oral and Maxillofacial Surgery, University of Tübingen, Tübingen, Germany.
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MeSH Terms
Descriptor/Qualifier:
Abnormalities, Multiple*
Child
Facies
Growth Disorders / complications*
Humans
Male
Malocclusion / complications
Maxillofacial Abnormalities / complications*
Mental Retardation / complications*
Odontogenic Cysts / complications*,  surgery
Syndrome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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