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Up to: Hereditary disease · Dental enamel hypoplasia

Amelogenesis imperfecta

Amelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body.

3 trials tagged with this condition →

Hypocalcified amelogenesis imperfecta 0 trials · 3 incl. sub-types Sub-types →
Amelogenesis imperfecta type 1G 1 trial
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 0 trials
Amelogenesis imperfecta type 1 0 trials Sub-types →
Amelogenesis imperfecta type 2 0 trials Sub-types →
Amelogenesis imperfecta, IIa 1K 0 trials
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism 0 trials