Amelogenesis imperfecta is a rare condition that affects the formation of enamel ( amelogenesis ).
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Amelogenesis imperfecta is a rare condition that affects the formation of enamel ( amelogenesis ).
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Mutations in the related AMELX gene on the X chromosome cause X-linked amelogenesis imperfecta.
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This is because they are formed by entrapment of odontoblast processes between ameloblasts prior to and during amelogenesis.
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His thesis was'A histological investigation of amelogenesis in rats, with special reference to maturation '.
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Amelogenesis, or enamel formation, occurs after the first establishment of dentin, via cells known as ameloblasts.
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Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome ( TDO ) and amelogenesis imperfecta with taurodontism.
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A mutation in FAM20A was reported to be associated with amelogenesis imperfecta, an inherited enamel defect, and gingival hyperplasia syndrome.
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About 5 % of amelogenesis imperfecta cases are caused by mutations in the AMELX gene and are inherited in an X-linked pattern.
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The protein Amelogenin is a type of extracellular matrix protein, and is involved in the progcess of amelogenesis, the formation of enamel on teeth.
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