amelogenesis imperfecta
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 ...
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Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta
... Amelogenesis imperfecta (AI) is a genetically heterogeneous group of diseases that result in defective development of tooth enamel. Mutations in several enamel proteins and proteinases have been associated ...
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Full Mouth Rehabilitation in a Patient with Amelogenesis Imperfecta: Treatment for Aesthetic and Functional Improvement
... of amelogenesis imperfecta along with palatally positioned maxillary lateral incisors with the use of porcelain bonded to metal FPDs and full ceramic, porcelain bonded to metal and full metal crowns to ...
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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 ...during amelogenesis. The pivotal role of AMBN in amelogenesis ...
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Functional and Esthetic Rehabilitation of a Young Patient with Amelogenesis Imperfecta
... Amelogenesis imperfecta (AI) is a hereditary disorder that expresses a group of conditions that cause developmental alterations in the structure of ...
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Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta
... Amelogenesis Imperfecta (AI) is the collective term given to a genetically heterogeneous group of inherited defects of tooth enamel biomineralisation. Typically all teeth of the primary and secondary ...
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Novel genetic linkage of rat Sp6 mutation to Amelogenesis imperfecta
... Amelogenesis imperfecta is an inherited disorder of enamel formation with both clinical and genetic hetero- geneity ...in amelogenesis could promote the development of the therapeutic application, ...
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A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta
... exchanger, as a cause of amelogenesis imperfecta. Am. J. Hum. Genet., 92, 307-312. 12 Parry, D.A., Brookes, S.J., Logan, C.V., Poulter, J.A., El-Sayed, W., Al- Bahlani, S., Al Harasi, S., Sayed, J., Raif ...
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Skeletal open bite with amelogenesis imperfecta treated with compression osteogenesis: a case report
... Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, that affect the structure and clinical appearance of enamel of all or nearly all teeth in a generally ...
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Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate
... Inherited diseases caused by genetic mutations can arise due to loss of protein function. Alternatively, mutated proteins may mis-fold, impairing endoplasmic reticulum (ER) trafficking, causing ER stress and triggering ...
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Amelogenesis Imperfecta: A Multidisciplinary Approach for Esthetic and Functional Full-mouth Comprehensive Rehabilitation
... How to cite this article: Allappanavar KS, Kiran Kumar N, Shaktidar PR. Amelogenesis Imperfecta: Multidisciplinary Approach for Esthetic and Functional Full-mouth Comprehen- sive Rehabilitation. Int J Prev ...
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Enamel defects in extracted and exfoliated teeth from patients with Amelogenesis Imperfecta, measured using the extended enamel defects index and image analysis
... Design: The sample comprised 109 deciduous and 7 permanent teeth from 32 individuals of 19 families with Amelogenesis Imperfecta in Northern Sweden. A special holder for individual teeth was designed and ...
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Enamel defects in extracted and exfoliated teeth from patients with Amelogenesis Imperfecta, measured using the extended enamel defects index and image analysis
... The sample comprised 109 deciduous and 7 permanent anterior and posterior teeth collected by one of the authors in Northern Sweden from 32 individuals of 19 families with Amelogenesis Imperfecta 23 . The ...
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Mutation Screening of ENAM, KLK4, MMP20 and FAM83H Genes among the Members of Five Iranian Families Affected with Autosomal Recessive Hypoplastic Amelogenesis Imperfecta
... Amelogenesis Imperfectas (AIs) are clinically and genetically heterogeneous conditions characterized by a wide range of clinical features. These abnormalities of enamel formation are categorized into three main ...
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Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta
... T HE ASSOCIATION OF AMELOGENESIS IMPERFECTA AI with cone-rod dystrophy CORD was originally described in a consanguineous Arabic family with 29 affected members, who resided in the Gaza s[r] ...
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Amelogenesis Imperfecta: Clinical and Consanguinity Study
... Amelogenesis imperfecta is considered a heterogeneous group of genetic disorders that cause developmental alterations in the structure of dental enamel ...
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“PERFECTING THE IMPERFECTA” CASE REPORT ON AMELOGENESIS IMPERFECTA
... earlier and more comprehensive than for others. Various treatment approaches have been described for rehabilitation of amelogenesis imperfecta in adults and children. 11 The use of composite resins in ...
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Interdisciplinary treatment approach for a young patient with amelogenesis imperfecta and anterior open bite
... Amelogenesis imperfecta (AI) is defined as a hereditary disorder expressing a group of conditions that cause developmental alterations in the structure of enamel (Neville et The enamel defects are highly ...
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A Conservative Rehabilitation of Amelogenesis Imperfecta
... Children with Amelogenesis Imperfecta (AI) experience many oral difficulties including sensitivity and aesthetics. Early recognition followed by appropriate preventive care and oral rehabilitation is ...
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Amelogenesis Imperfecta caused by N-Terminal Enamelin Point Mutations in Mice and Men is driven by Endoplasmic Reticulum Stress
... Inherited defects of dental enamel biomineralization, amelo- genesis imperfecta (AI; MIM PS104500), constitute a common group of genetic diseases that occur with an incidence as high as 1:700 live births (4). ...
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