However, three patients reported with a mutation in TCF12 (Family 31, Individual II‐1 in Supplementary Table SIII in Sharma et al. [2013] Probands 1 and 2 in Paumard‐Hernandez et al., 2014) had hearing loss suggesting that hearing loss might be an occasional feature of TCF12‐related syndrome, as it is of other craniosynostosis syndromes. This evidence concerns the gene TCF12 and syndromic craniosynostosis.