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...

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Detalles Bibliográficos
Autores principales: Li, Xiaojing, Ye, Xiaowei, Su, Jimei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
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

Internet

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

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