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Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis.

Pediatric research - 1 May 2024

Faria-Teixeira Maria Cristina, Tordera Cristina, Salvado E Silva Francisco, Vaz-Carneiro António, Iglesias-Linares Alejandro

Abstract excerpt

Skeletal Class III (SCIII) is among the most challenging craniofacial dysmorphologies to treat. There is, however, a knowledge gap regarding which syndromes share this clinical phenotype. The aims of this study were to: (i) identify the syndromes affected by the SCIII phenotype; (ii) clarify the involvement of maxillary and/or mandibular structures; (iii) explore shared genetic/molecular mechanisms. A two-step...

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PMID: 38347173
DOI: 10.1038/s41390-023-02907-5
PMCID: PMC11126392

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