Document Detail


Oral findings in Rett syndrome: a systematic review of the dental literature.
MedLine Citation:
PMID:  20526264     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developmental regression, particularly in relation to expressive language and use of the hands, together with profound mental retardation, that almost exclusively affects females. The present review describes the 35 cases of RS published in the indexed literature (Medline)--the first corresponding to 1985 and the last to the year 2007. Certain oral manifestations of the disease are derived from the drug treatment prescribed to control the disease, while others are common to other clinical conditions characterized by convulsion activity, difficulties for correct oral hygiene, walking problems and/or an excess of oral/digital-manual habits. In any case, bruxism is the oral habit most frequently associated with RS--the treatment of which remains the subject of controversy.
Authors:
María-Cristina Fuertes-González; Francisco-Javier Silvestre; José-Manuel Almerich-Silla
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Publication Detail:
Type:  Journal Article     Date:  2011-01-01
Journal Detail:
Title:  Medicina oral, patología oral y cirugía bucal     Volume:  16     ISSN:  1698-6946     ISO Abbreviation:  Med Oral Patol Oral Cir Bucal     Publication Date:  2011 Jan 
Date Detail:
Created Date:  2010-12-30     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101231694     Medline TA:  Med Oral Patol Oral Cir Bucal     Country:  Spain    
Other Details:
Languages:  eng     Pagination:  e37-41     Citation Subset:  D; IM    
Affiliation:
Red Cross Dental Clinic for Special Patients, Valencia, Spain.
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