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Concept information

Stomatognathic Diseases > Tooth Diseases > Tooth Abnormalities > Dental Enamel Hypoplasia
Stomatognathic Diseases > Stomatognathic System Abnormalities > Tooth Abnormalities > Dental Enamel Hypoplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Stomatognathic System Abnormalities > Tooth Abnormalities > Dental Enamel Hypoplasia

Terme préférentiel

Dental Enamel Hypoplasia  

Type

  • mesh:Descriptor

Définition

  • An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors. A type of developmental disturbance of AMELOGENESIS involving permanent INCISORS and first permanent MOLARS. It is characterized by asymmetrical enamel defects with severe hypomineralization.

Concept générique

Concepts spécifiques

Synonyme(s)

  • Enamel Agenesis
  • Enamel Hypoplasia
  • Enamel Hypoplasia, Dental
  • Hypoplasia, Dental Enamel
  • Hypoplastic Enamel

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-BGQ0MRMV-L

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RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 30/06/2018