Cargando…
Binder's phenotype with ankyloglossia: Report of a rare inherited association in an Indian female
Binder's syndrome, a rare congenital malformation of nasomaxillary complex, first described in 1962, has a hexad of characteristic clinical and radiographic features consisting of arhinoid face, intermaxillary hypoplasia with malocclusion, abnormal position of nasal bones, atrophy of nasal muco...
| Autores principales: | , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer - Medknow
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017849/ https://www.ncbi.nlm.nih.gov/pubmed/35450230 http://dx.doi.org/10.4103/jomfp.jomfp_143_21 |