amelogenesis


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amelogenesis

 [ah-mel″o-jen´ĕ-sis]
formation of dental enamel.
amelogenesis imperfec´ta a hereditary disease in which there is imperfect formation of enamel, resulting in brownish coloration and friability of the teeth.

am·e·lo·gen·e·sis

(am'ĕ-lō-jen'ĕ-sis),
The deposition and maturation of enamel.
Synonym(s): enamelogenesis

amelogenesis

(ăm′ə-lō-jĕn′ĭ-sĭs)
n.
The formation and development of dental enamel.

am·e·lo·gen·e·sis

(am'ĕ-lō-jen'ĕ-sis)
The deposition and maturation of enamel.
Synonym(s): enamelogenesis.

am·e·lo·gen·e·sis

(am'ĕ-lō-jen'ĕ-sis)
The deposition and maturation of enamel.
Synonym(s): enamelogenesis.
References in periodicals archive ?
X-linked hypomaturation type of amelogenesis imperfecta exhibiting lionization in females.
Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype.
Based on clinical and radiographic features, a diagnosis of hereditary Amelogenesis imperfecta was made and the objectives of the treatment planned were to preserve the tooth structure, improve esthetics and masticatory function.
The molecular etiologies and associated phenotypes of amelogenesis imperfecta.
Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.
That open-bite is related to calculus accumulation, might contribute also to the calculus accumulation in children with amelogenesis imperfecta who present with open-bite [Stewart et al., 1982].
This anomaly is differentiated from amelogenesis imperfecta and dentinogenesis imperfecta because it appears unilaterally (PANDIS et al., 1991) and is not generalized.
El marcador mas clasico es la presencia de hipoplasia del esmalte que refleja fallos en la amelogenesis que se manifiestan como bandas transversales rehundidas en la superficie de las piezas dentales.
During amelogenesis, ingested low levels of fluoride (from food, water, or supplements) can replace the hydroxyl group in some of the hydroxyapatite crystals.
y otros cuatro autores; Efectos del grabado acido en la amelogenesis imperfecta hipomineralizada: Estudio microscopico y microanalitico.
Set C includes exons 9, 13, 16, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 48, 60, 69, 72, and 74, plus an amplicon for the AMELX gene [amelogenin (amelogenesis imperfecta 1, X-linked)] when required.