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• 14:38, 3 February 2024 Fmichael1 talk contribs created page Apert Syndrome (Created page with "= Key features = * thumbCaused by FGFR2 mutation, AD inherited * Incidence ~1:65,000 * Bicoronal craniosynostosis, midfacial retrusion, exorbitism & severe hand/foot anomaly. * Pathognomonic feature - severe & complex fusion of fingers & toes (complex syndactyly). * Craniofacial features:  craniosynostosis, turribrachycephaly, hypertelorism, midfacial retrusion, cleft palate & down-slanted palpebral fissures. * May also have: cleft palate, p...") Tag: Visual edit