Amelogenesis imperfecta, type 3A
MONDO:0007538Any amelogenesis imperfecta in which the cause of the disease is a mutation in the FAM83H gene.
Also known as: amelogenesis imperfecta hypomineralization type, amelogenesis imperfecta type 3, amelogenesis imperfecta type III, ADHCAI, AI3, FAM83H amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in FAM83H, amelogenesis imperfecta, type 3A
4 clinical trials for this condition and its sub-types.
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Vitamin d mouthwash shows promise for Kids' chalky teeth
Disease control CompletedThis study tested whether a vitamin D mouthwash can help repair weak spots on children's permanent teeth (a condition called molar incisor hypomineralization) and improve gum health. Thirty-two children over age 6 used either a vitamin D or placebo mouthwash. Researchers measured…
Phase: PHASE1 • Sponsor: Cairo University • Aim: Disease control
Last updated Jul 08, 2026 00:00 UTC
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Quick lesson boosts Dentists-in-Training on tricky tooth condition
Knowledge-focused CompletedThis study tested whether a 30-minute interactive lesson could improve dental interns' understanding of Molar-Incisor Hypomineralization (MIH), a condition that causes weak spots on teeth. Two hundred dental interns from Future University in Egypt took a quiz before and after the…
Phase: NA • Sponsor: Future University in Egypt • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:57 UTC