Síndrome del incisivo central único de la línea media del maxilar y fusión de incisivos centrales permanentes mandibulares: Reporte de un caso clínico
The solitary median maxillary central incisor syndrome is not a very frequent anomaly, and is characterized mainly by structural malformations of the craniofacial area. The most significant clinical characteristic is in the oral cavity, with the presence of a unique incisor enveloped in the half lin...
| Autores: | , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2022 |
| País: | México |
| Institución: | UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO |
| Repositorio: | Revista Odontológica Mexicana |
| Idioma: | español |
| OAI Identifier: | oai:ojs.pkp.sfu.ca:article/16066 |
| Acceso en línea: | https://revistas.unam.mx/index.php/rom/article/view/16066 |
| Access Level: | acceso abierto |
| Palabra clave: | Solitary median incisor single median maxillary central incisor Incisivo central único medial del maxilar |
| Sumario: | The solitary median maxillary central incisor syndrome is not a very frequent anomaly, and is characterized mainly by structural malformations of the craniofacial area. The most significant clinical characteristic is in the oral cavity, with the presence of a unique incisor enveloped in the half line of the maxillary in both dentitions (primary and permanent). This report describes a 6 year old girl with a unique incisor enveloped in the half line of the maxillary and other abnormalities were detected: absence of the labial frenulum, fusion of central teeth and oval palate. The presence of the unique incisor will always be associated to other anomalies, such as: deficit of growth hormone and Triple X syndrome; besides being considered a holoprosencephaly predictor. |
|---|