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Article

Abnormalities in pharyngeal arch-derived structures in SATB2-associated syndrome.

Clinical genetics - 1 Aug 2024

Zarate Yuri A, Bosanko Katherine, Derar Nada, Fish Jennifer L

Abstract excerpt

SATB2-associated syndrome (SAS, glass syndrome, OMIM#612313) is a neurodevelopmental autosomal dominant disorder with frequent craniofacial abnormalities including palatal and dental anomalies. To assess the role of Satb2 in craniofacial development, we analyzed mutant mice at different stages of development. Here, we show that Satb2 is broadly expressed in early embryonic mouse development including the...

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Identifiers

PMID: 38693682
DOI: 10.1111/cge.14540
PMCID: PMC11216868

Genes

SATB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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