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Amelogenesis imperfecta, type IB

*Gene map locus 4q21
AI1B
AIH2
Amelogenesis imperfecta, hypoplastic local, autosomal dominant
Enamel hypoplasia, hereditary localized
[Clinical features: hypoplastic amelogenesis imperfecta; horizontal row of pits, linear depressions, or one large hypoplastic area in the enamel with hypocalcification of the enamel adjacent to and below the hypoplastic area]
[Inheritance: autosomal dominant]

Autosomal-dominant Hypoplastic Form of Amelogenesis Imperfecta Caused by an Enamelin Gene Mutation at the Exon-Intron Boundary
Phenotype of ENAM Mutations is Dosage-dependent
Phenotype of ENAM Mutations is Dosage-dependent
Journal of Dental Research
Journal of Dental Research
Journal of Dental Research


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Edited by Aldo Campana, August 21, 2012