Cargando…
The dental phenotype of primary dentition in SATB2-associated syndrome: a report of three cases and literature review
BACKGROUND: SATB2-associated syndrome (SAS; OMIM: 612,313) is an autosomal dominant inherited multisystemic disorder caused by several variants of the SATB2 gene. SAS is characterized by intellectual disability, developmental delay, severe speech anomalies, craniofacial anomalies, and dental abnorma...
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9717407/ https://www.ncbi.nlm.nih.gov/pubmed/36457071 http://dx.doi.org/10.1186/s12903-022-02594-4 |