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Dental treatment in Angelman syndrome patients. 8 Case reports
 

Type:  Articles

Pubblication date:  12/2012

Authors:  C. Gallo, A. Marcato, M. Beghetto, E. Stellini*

Language:  English

Institution:  Department of Community Dentistry – Piove di Sacco Hospital – ULSS 16 Padua *Unit of Paediatric Dentistry– University of Padua, Padova, Italy

Publication:  European Journal of Paediatic Dentistry

Publisher:  Ariesdue Srl

Keywords:  Angelman syndrome; Dental treatment; Rare syndrome.

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Email:  claudio.gallo@sanita.padova.it


Title:  Dental treatment in Angelman syndrome patients. 8 Case reports

Abstract:  Background Angelman syndrome is a rare neurogenetic disorder resulting in delayed neuropsychological development, intellectual disability, speech impairment, movement or balance disorder and a behavioural uniqueness. It is caused by deletion of maternal chromosome 15q11-13. The syndrome has oral manifestations such as diastemas, tongue thrusting, sucking/swallowing disorder, mandibular prognathism, and wide mouth. The dental literature on the syndrome is scarce. Case report We report our approach to dental procedures in Angelman syndrome patients, and the relationship between the dental staff and the patient and his family. The purpose of this paper is to highlight the possibility of dental treatment in general anaesthesia, due to the lack of cooperation of some of these patients.

 
 
 
 
 
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