Hypoplastic amelogenesis imperfecta with multiple impacted teeth: report of two cases [PDF]
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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Bilateral taurodontism in primary and permanent molars associated with hypodontia
The article is to present a case of bilateral taurodontism in primary and permanent molars associated with hypodontia and to discuss the endodontic aspects.
Parmeshwarappa Poornima +3 more
doaj +1 more source
Prevalence and distribution of selected dental anomalies among saudi children in Abha, Saudi Arabia [PDF]
Dental anomalies are not an unusual finding in routine dental examination. The effect of dental anomalies can lead to functional, esthetic and occlusal problems.
Yassin, Syed M.
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Taurodontism in simultaneous existence with multiple supernumerary teeth: A case report
Supernumerary teeth and taurodontism are both common dental anomalies when found as isolated entities. However, simultaneous presence in the same individual without a syndrome is rarely reported in the literature. This case report describes a 20-year-old
Dena Yakoup +2 more
doaj +1 more source
Background: Molar incisor hypomineralisation (MIH) is a common disorder of tooth development, which has recently been found to be associated with a higher prevalence of hypodontia.
Helen D. Rodd +19 more
doaj +1 more source
Genetic basis of dental agenesis - molecular genetics patterning clinical dentistry [PDF]
Tooth agenesis is one of the most common congenital malformations in humans. Hypodontia can either occur as an isolated condition (non-syndromic hypodontia) or can be associated with a syndrome (syndromic hypodontia), highlighting the heterogeneity of ...
Chhabra, Anuj +2 more
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Endodontic treatment of a hypertaurodont mandibular second molar with C-shaped canal: A case report
Taurodontism is a variation in tooth anatomy characterized by an enlarged pulp chamber with hypertaurodont being its most severe presentation. The complexity of endodontic treatment of hypertaurodont tooth may be compounded by coexistent C-shaped canal ...
Shaikh Shahbaz +3 more
doaj +1 more source
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta [PDF]
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 with AI.
Maria CLG Santos +47 more
core +2 more sources
Bulls′ teeth: An insight through CBCT
Taurodontism is a morphologic alteration in the shape of the tooth, in which there is an enlargement of the pulp chamber with apical displacement of the pulpal floor and lack of the normal constriction at the level of the cemento-enamel junction ...
Anjali Gupta +3 more
doaj +1 more source
A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate ΔNp63α. [PDF]
The homeodomain transcription factors play crucial roles in many developmental processes ranging from organization of the body plan to differentiation of individual tissues.
Calabrò V. +7 more
core +1 more source

