Hypoplastic amelogenesis imperfecta with multiple impacted teeth: report of two cases [PDF]
, 2010 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.
Aarthi Nisha, Aarthi +2 more
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Kohlschütter-Tönz Syndrome: report of an additional case [PDF]
, 2013 Kohlschütter-Tönz Syndrome is a rare disorder clinically characterized by amelogenesis imperfecta, epilepsy and progressive mental deterioration. We present an additional case of this syndrome of a nine year-old boy who was referred by pigmented teeth ...
Almeida, Oslei Paes de +4 more
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Advances in Mechanical Engineering, 2015 Hypoplastic amelogenesis imperfecta is a widespread hereditary disease that causes the loss of enamel. The purpose of this study was to investigate the nanoscratch resistance of hypoplastic amelogenesis imperfecta for providing a reference for ...
Ping Qing +5 more
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Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations [PDF]
, 2014 Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects. Commonly described as an isolated trait, it may be observed concomitantly with other orodental and/or systemic features such as ...
Acevedo, A-C +8 more
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A secretory kinase complex regulates extracellular protein phosphorylation. [PDF]
, 2015 Although numerous extracellular phosphoproteins have been identified, the protein kinases within the secretory pathway have only recently been discovered, and their regulation is virtually unexplored.
Cui, Jixin +5 more
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Amelogenesis imperfecta and localised aggressive periodontitis: A rare clinical entity
Journal of Indian Society of Periodontology, 2013 This case report presents two female patients whose chief complaint was discoloration of teeth. On careful clinical examination it was found that the patients had features of amelogenesis imperfecta and localised aggressive periodontitis.
Gayatri Gundannavar +3 more
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Amelogenesis Imperfecta caused by N-Terminal Enamelin Point Mutations in Mice and Men is driven by Endoplasmic Reticulum Stress [PDF]
, 2017 ‘Amelogenesis imperfecta’ (AI) describes a group of inherited diseases of dental enamel that have major clinical impact. Here, we identify the aetiology driving AI in mice carrying a p.S55I mutation in enamelin; one of the most commonly mutated proteins ...
Alan J. Mighell +58 more
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Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta [PDF]
, 2014 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.
Brookes, SJ +8 more
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Prosthodontic rehabilitation: Cutting edge treatment for amelogenesis imperfecta
Indian Journal of Dental Sciences, 2022 Amelogenesis imperfecta is a genetically determined inherited disorder characterized by abnormal formation of tooth enamel leading to esthetic, functional, and psychological impact on the patient.
Saurav Banerjee, Debabrata Biswas
doaj +1 more source
Abnormalities in enamel structure and their association with systemic diseases and syndromes [PDF]
, 2011 Etiology of abnormalities in tooth structure has been subject of numerous studies but still has not been fully understood. Heredity is an established etiological factor for many types of structural anomalies of the teeth. Factors that cause changes in
Babić Marko +4 more
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