Noonan syndrome: A case report.
Eur J Paediatr Dent
; 11(2): 97-100, 2010 Jun.
Article
em En
| MEDLINE
| ID: mdl-20635845
ABSTRACT
AIM:
Noonan syndrome is a rare genetic alteration; the responsible gene is located on the long arm of chromosome 12. CASE REPORT The authors examined a caucasic girl of eight years with Noonan syndrome. The patient had systemic problems, such as otitis, heart trouble, language disturbances and asymmetry of the lower limbs. Light mental delay was also found. She had the bad habit of sucking the lower lip. The treatment plan was extraction of some teeth, sealing of first molars and orthodontic treatment with functional appliance.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Má Oclusão
/
Síndrome de Noonan
Tipo de estudo:
Etiology_studies
Limite:
Child
/
Female
/
Humans
Idioma:
En
Revista:
Eur J Paediatr Dent
Assunto da revista:
ODONTOLOGIA
/
PEDIATRIA
Ano de publicação:
2010
Tipo de documento:
Article