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• W2034351012 abstract "Craniosynsostosis syndromes exhibit considerable phenotypic and genetic heterogeneity. Sagittal synostosis is common form of isolated craniosynostosis. The sutures involved, the shape of the skull and associated malformations give a clue to the specific diagnosis. Crouzon syndrome is one of the most common of the craniosynostosis syndromes. Apert syndrome accounts for 4.5% of all craniosynostoses and is one of the most serious of these syndromes. Most syndromic craniosynostosis require multidisciplinary management. The following review provides a brief appraisal of the various genes involved in craniosynostosis syndromes, and an approach to diagnosis and genetic counseling." @default.
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• W2034351012 date "2011-01-01" @default.
• W2034351012 modified "2023-10-02" @default.
• W2034351012 title "Craniosynostosis genetics: The mystery unfolds" @default.
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• W2034351012 doi "https://doi.org/10.4103/0971-6866.86171" @default.
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