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Chin J Dent Res ; 27(1): 29-38, 2024 Mar 28.
Artículo en Inglés | MEDLINE | ID: mdl-38546517

RESUMEN

Non-syndromic orofacial clefts (NSOCs) are the most common craniofacial malformation. In the complex aetiology and pathogenesis of NSOCs, genetic factors play a crucial role and IRF6, located at chromosome 1q32.2, is the best documented NSOC susceptibility gene. IRF6 is a key factor in oral maxillofacial development and known to contribute the most in NSOCs. It is essential to conduct a complete review of the existing results on IRF6 to further understand its role in the pathogenesis of NSOCs. Thus, the present authors summarised the research progress on the mechanism of IRF6 in NSOCs from both genetic and functional perspectives in this review.


Asunto(s)
Labio Leporino , Fisura del Paladar , Humanos , Labio Leporino/genética , Fisura del Paladar/genética , Cromosomas Humanos Par 2 , Desarrollo Maxilofacial , Factores Reguladores del Interferón/genética
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