Non-Syndromic Familial Mesiodens: Presentation of Three Cases

Primer Autor
Fuentes, Ramon
Co-autores
Alarcon, Josefa
Guzman, Jacob
Masuko, Telma S.
Navarro Caceres, Pablo
Título
Non-Syndromic Familial Mesiodens: Presentation of Three Cases
Editorial
MDPI
Revista
DIAGNOSTICS
Lenguaje
en
Resumen
Mesiodens are the most common supernumerary teeth and are detected incidentally during routine radiographic examination, so late diagnosis complications are very common. The dentist must make a timely diagnosis and thus avoid clinical complications. Despite advances in knowledge of dental morphogenesis and differentiation, the etiology of mesiodens remains unclear. Therefore, several theories have been postulated to explain how and why they develop. It was described in the literature that heredity could play an important role in the appearance of supernumerary teeth, with a higher rate of appearance in relatives of those affected. This article reports three cases, a mother and two children, who present mesiodens, which shows that supernumerary teeth may involve a genetic factor. In addition, a literature review was carried out to assess the importance of the genetic factor as a possible cause of mesiodens. The relevance and implications of timely diagnosis in clinical practice to avoid manifestations of clinical complications are discussed. Therefore, the identification of the genetic risk factors responsible for the formation of supernumerary teeth is essential for developing a screening tool to determine an individual's genetic risk.
Tipo de Recurso
artículo original
doi
10.3390/diagnostics12081869
Formato Recurso
PDF
Palabras Claves
supernumerary teeth
diagnosis
genetics
complications
SUPERNUMERARY TEETH
INCISORS
Ubicación del archivo
Categoría OCDE
Medicina general e interna
Materias
dientes supernumerarios
diagnosis
genética
complicaciones
DIENTES SUPERNUMERARIOS
INCISORES
Disciplinas de la OCDE
Odontología, Cirugía y Medicina Oral
Genética y Herencia
Otros Temas de Medicina Clínica
Título de la cita (Recomendado-único)
Non-Syndromic Familial Mesiodens: Presentation of Three Cases
Identificador del recurso (Mandatado-único)
artículo original
Versión del recurso (Recomendado-único)
version publicada
License
CC BY 4.0
Condición de la licencia (Recomendado-repetible)
CC BY 4.0
Derechos de acceso
acceso abierto
Access Rights
acceso abierto
Id de Web of Science
WOS:000846099500001
Revisa las metricas alternativas de Almetrics
Revisa las citaciones de Dimensions