Results 131 to 140 of about 6,152 (269)
Citation: 'oligodontia' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.11031 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
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A Novel PAX9 Mutation in a Family with Non-Syndromic Oligodontia [PDF]
Ye Ji Lee +5 more
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Mechanisms and molecular regulation of mammalian tooth replacement [PDF]
In most non-mammalian vertebrates, such as fish and reptiles, teeth are replaced continuously. However, tooth replacement in most mammals, including human, takes place only once and further renewal is apparently inhibited.
Järvinen, Elina
core
Congenital malformations [PDF]
Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or during the intrauterine life. Their global birth prevalence is about 2–3%.
CORSELLO, Giovanni, GIUFFRE, Mario
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Dystrophic epidermolysis bullosa associated with non-syndromic hypodontia
Epidermolysis bullosa (EB) is a genetic disease associated with fragility and bullous lesions of the skin and mucous membranes. There are various patterns of inheritance and histopathology. The disease is associated with systemic and oral manifestations,
Sonali Sharma, Sumit Bedi
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Oral rehabilitation of non-syndromic oligodontia: A case report [PDF]
Manoranjan Mahakur +6 more
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Agenesia dos incisivos laterais superiores: prevalência, diagnóstico e tratamento [PDF]
A agenesia dentária é uma das anomalias mais comuns da dentição humana, afectando 20% da população mundial, já a agenesia dos incisivos laterais superiores afecta 2% conforme a população estudada.
Moreira, Fernanda Alves
core
Dental Rehabilitation in Class III Anomaly with Oligodontia after Palatal Distraction and Osteotomy under Cone-Beam CT Assistance [PDF]
Manfred Nilius +2 more
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Non syndromic oligodontia: case report.
Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes.
Tangade, Pradeep, Batra, Manu
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