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Supernumerary teeth in a patient with Turner syndrome: An unusual finding.
Andrade, Natália Silva; Tenório, Jefferson R; Gallottini, Marina.
  • Andrade NS; Special Care Center, School of Dentistry, University of São Paulo, São Paulo, São Paulo, Brazil.
  • Tenório JR; Special Care Center, School of Dentistry, University of São Paulo, São Paulo, São Paulo, Brazil.
  • Gallottini M; School of Dentistry, Special Care Center, University of São Paulo, São Paulo, São Paulo, Brazil.
Spec Care Dentist ; 39(5): 538-542, 2019 Sep.
Article en En | MEDLINE | ID: mdl-31361348
ABSTRACT

AIMS:

Turner syndrome (TS) is a genetic disorder associated with abnormalities of the X-chromosome, occurring in about 1 in 2000 to 1 in 3000 live-born girls. We present a case of a 14-year-old girl with TS, who was referred to our outpatient clinic in 2016 because of an ectopic eruption. METHODS AND

RESULTS:

Dental clinical examination and radiographic investigation revealed eight supernumerary teeth, short roots, enamel hypoplasia, increased overjet, rotation and displacement of teeth, moderate gingivitis and morphological alteration of the upper right central incisor. Dental treatment included extraction of erupted supernumerary teeth, composite resin restoration, supragingival scaling and oral hygiene for plaque control.

CONCLUSIONS:

The unpublished finding of supernumerary teeth in our patient has led us to suggest the investigation of this dental developmental anomaly in other patients with Turner syndrome.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diente Supernumerario / Síndrome de Turner / Hipoplasia del Esmalte Dental / Anomalías de la Boca Tipo de estudio: Diagnostic_studies Límite: Adolescent / Female / Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diente Supernumerario / Síndrome de Turner / Hipoplasia del Esmalte Dental / Anomalías de la Boca Tipo de estudio: Diagnostic_studies Límite: Adolescent / Female / Humans Idioma: En Año: 2019 Tipo del documento: Article