The dental phenotype of primary dentition in SATB2-associated syndrome: a report of three cases and literature review

Abstract 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...

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Principais autores:	Xiaojing Li, Xiaowei Ye, Jimei Su
格式:	Artigo
语言:	Inglês
出版:	BMC 2022-11-01
丛编:	BMC Oral Health
主题:	SATB2-associated syndrome SATB2 gene Dental abnormalities
在线阅读:	https://doi.org/10.1186/s12903-022-02594-4
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