: MeSH: Dental Enamel Hypoplasia

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

Dental Enamel Hypoplasia

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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.

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