Teeth are specialized structural components of the craniofacial skeleton. Developmental defects occur either alone or in combination with other birth defects. In this paper, we review the dental anomalies in several multiple congenital anomaly (MCA) syndromes, in which the dental component is pivotal in the recognition of the phenotype and/or the molecular basis of the disorder is known. We wil...

The purpose of this study was to determine the prevalence of developmental dental anomalies in an Indian population and to statistically analyze the distribution of these anomalies. The study was based on clinical examination, evaluation of dental casts, and panoramic radiographs of 1123 Indian subjects (572 males, 551 females), who visited the outpatient clinic at Government Dental College, In...

Background Variants in DLX3 cause tricho-dento-osseous syndrome (TDO; MIM accession no. 190320), a systemic condition with hair, nail, and bony changes, taurodontism, amelogenesis imperfecta (AI) inherited an autosomal dominant fashion. Different variants found within this gene are associated different phenotypic presentations. To date, 6 have been reported TDO. The aim of paper is to explore d...

The aim of this study was to determine the prevalence and incidence evaluate current status dental treatment Amelogenesis imperfecta (AI) Dentinogenesis (DI) in South Korea. data based on National Health Insurance Service (NHIS)-National Sample Cohort Database (2002 - 2015) Jeonbuk University (JBNU) Dental Hospital (2011 2020). NHIS analysis showed AI DI were 11.6 2.4 per 100,000 people, respec...

Objectives Amelogenesis imperfecta (AI) comprises a clinically and genetically heterogeneous group of conditions that affects the dental enamel, occasionally in conjunction with other dental, oral, and extra oral tissues. The purpose of this case report was to describe the necessity of the multidisciplinary approaches taken to treat a young patient diagnosed with hypocalcified-type of amelogene...