Multidisciplinary treatment of non-syndromic oligodontia [PDF]
European Journal of Dentistry, 2012 ABSTRACTOligodontia is the agenesis of 6 or more teeth, excluding third molars. The etiology of congenital absence of teeth is believed to be rooted in heredity or developmental anomalies. The absence of teeth in patients can cause aesthetic, functional, and psychological problems, particularly if the anterior region is involved.
Evren Öztaş, Canan Bural
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Familial non-syndromic oligodontia
Journal of Indian Academy of Oral Medicine and Radiology, 2015 Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer.
Seema Basoya +3 more
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NON-SYNDROMIC CONGENITAL, OLIGODONTIA: MANAGEMENT OF A CASE IN A NIGERIAN CHILD [PDF]
Journal of IMAB, 2019 Congenitally missing teeth (CMT) may present as complete (Anodontia) or partial (Hypodontia or Oligodontia) depending on the number of teeth missing.
Enoch Abiodun Idowu +3 more
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Triad of Micrognathia, Oligodontia, and Ankyloglossia in a Non-Syndromic Individual: A Case Report with Rare Presentation [PDF]
Journal of Pharmacy and Bioallied SciencesDeviations from the normal in the intrauterine formative phase have a permanent effect in an individual’s life. They can cause limitations in lifestyle from nil to severe. The sites may differ and hence would the presentations.
Priti Shukla +3 more
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Treatment strategy for patient with non-syndromic tooth agenesis: a case report and literature review [PDF]
BMC Oral HealthBackground Non-syndromic tooth agenesis (NSTA) is a type of ectodermal dysplasia (ED) in which patients with non-syndromic oligodontia may only affect teeth. No pathological findings were found in other tissues of the ectodermal. Herein, we report a case
Tianfeng Ouyang +7 more
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Novel LRP6 Mutations Causing Non-Syndromic Oligodontia. [PDF]
J Pers Med, 2022 The process of tooth formation is a series of reciprocal interactions between the ectoderm and mesoderm, and it is believed that many genetic factors are involved in this complex process. More than a dozen genes have been identified in non-syndromic tooth agenesis; however, the genetic etiology underlying tooth agenesis is not fully understood yet.
Lee Y, Chae W, Kim YJ, Kim JW.
europepmc +3 more sources
Non-syndromic Oligodontia in Primary Dentition: A Report of a Rare Case. [PDF]
Cureus, 2023 The congenital absence of teeth is the most common dental anomaly affecting 2.2% to 10% of the population. It could be present in the form of anodontia, hypodontia, or oligodontia, excluding wisdom teeth. Oligodontia is most commonly associated with several syndromes like ectodermal dysplasia, Down syndrome, and Van der Woude syndrome that involve the ...
Badnaware S, Srivastava VK, Chandel M.
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Non-syndromic oligodontia in permanent dentition: a case report. [PDF]
Ghana Med J, 2014 Tooth agenesis is one of the most common congenital anomalies seen in humans. Although absence of one or more teeth is common but absence of multiple teeth is rare. Oligodontia is a rare developmental anomaly, involving agenesis of six or more permanent teeth, excluding the third molars.
Pannu P +3 more
europepmc +5 more sources
Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese families [PDF]
Molecular Genetics & Genomic MedicineWenjing Shen, Jiabao Ren, Ya Zhao
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Detection of a rare AXIN2 variant in an Iranian family with hypodontia and oligodontia [PDF]
Journal of Dental Research, Dental Clinics, Dental Prospects, 2022 Background. Hypodontia, or the absence of one or more teeth during tooth formation, is a highly prevalent dental anomaly. Nevertheless, the main causes are still unknown.
Shiva Safari +5 more
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