Taurodontism (Q85448): Difference between revisions
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Taurodontismo é uma anomalia dentária caracterizada por uma câmara pulpar alongada, deslocada em direção ao assoalho apical do dente sem constrição ao nível da junção cemento-esmalte, e raízes curtas. Afeta com mais frequência os dentes molares permanentes. Mais frequentemente acomete dentes molares permanentes. Taurodontismo aumenta o risco de exposição pulpar. Pode estar presente de forma isolada ou associada a algumas síndromes, como síndrome de Down, amelogênese imperfeita e síndrome de Klinefelter. | |||
| description / en | description / en | ||
Taurodontism is a dental anomaly characterised by an elongated pulp chamber, displaced toward the apical floor of the tooth with no constriction at the level of the cemento-enamel junction, and short roots. It most frequently affects permanent molar teeth. Taurodontism increases the risk of pulp exposure. It can be isolated or associated with certain syndromes such as Down syndrome, amelogenesis imperfecta, and Klinefelter syndrome. | |||
Revision as of 10:48, 15 August 2026
Taurodontism is a dental anomaly characterised by an elongated pulp chamber, displaced toward the apical floor of the tooth with no constriction at the level of the cemento-enamel junction, and short roots. It most frequently affects permanent molar teeth. Taurodontism increases the risk of pulp exposure. It can be isolated or associated with certain syndromes such as Down syndrome, amelogenesis imperfecta, and Klinefelter syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_356382747 |
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| English | Taurodontism |
Taurodontism is a dental anomaly characterised by an elongated pulp chamber, displaced toward the apical floor of the tooth with no constriction at the level of the cemento-enamel junction, and short roots. It most frequently affects permanent molar teeth. Taurodontism increases the risk of pulp exposure. It can be isolated or associated with certain syndromes such as Down syndrome, amelogenesis imperfecta, and Klinefelter syndrome. |
