The molecular etiologies and associated phenotypes of amelogenesis imperfecta

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[Amelogenesis imperfecta].

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Amelogenesis imperfecta

Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of 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. The prevalence varies from 1:700 to 1:14,000, according to the populations studied. Th...

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Amelogenesis Imperfecta- A Review

NTRODUCTION Amelogenesis Imperfecta (AI) is a developmental disorder of genomic origin, associated with abnormal enamel formation. Although AI is considered as a single disease entity, it actually represents a group of heterogeneous conditions, with diverse structural defects of enamel resulting in a range of clinical phenotypes. 1 It is characterized by clinical and genetic heterogeneity in th...

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Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta

Amelogenesis imperfecta (AI) describes a heterogeneous group of inherited dental enamel defects reflecting failure of normal amelogenesis. Ameloblastin (AMBN) is the second most abundant enamel matrix protein expressed during amelogenesis. The pivotal role of AMBN in amelogenesis has been confirmed experimentally using mouse models. However, no AMBN mutations have been associated with human AI....

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Amelogenesis Imperfecta: A Review of the Literature

Amelogenesis imperfecta (AI) is a hereditary group of disorder that causes disturbance in enamel formation resulting in developmental alterations of mineralization. Restoration of the dentition poses a great challenge when all the teeth are severely affected. The treatment opportunities for these patients may help in refining their lifestyle. The total treatment modality aims to relieve the pai...

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ژورنال

عنوان ژورنال: American Journal of Medical Genetics Part A

سال: 2006

ISSN: 1552-4825,1552-4833

DOI: 10.1002/ajmg.a.31358