Goldenhar syndrome with new oral findings!
Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocular and ear defects, hemifacial microsomia, and vertebral anomalies, which may also be associated with cardiovascular and renal malformations. It is a rare congenital anomaly of unclear etiology. The p...
Guardado en:
| Autor principal: | |
|---|---|
| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Wolters Kluwer Medknow Publications
2021
|
| Materias: | |
| Acceso en línea: | https://doaj.org/article/3db3425b016e402dae61131143cdd7b4 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
| Sumario: | Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocular and ear defects, hemifacial microsomia, and vertebral anomalies, which may also be associated with cardiovascular and renal malformations. It is a rare congenital anomaly of unclear etiology. The purpose of reporting this case of a 16-year-old boy with GS is, to update, the existing literature of new oral findings observed. |
|---|