Cerebral cortex maldevelopment in syndromic craniosynostosis.
Alexander T WilsonBianca K Den OttelanderMarie-Lise C Van VeelenMarjolein Hg DremmenJohn A PersingHenri A VroomanIrene Mj MathijssenRobert C TaskerPublished in: Developmental medicine and child neurology (2021)
Despite adequate ICV in FGFR-mediated craniosynostosis, CSA development is reduced, indicating maldevelopment, particularly in parietal and occipital lobes. Modified education is also more common in patients with FGFR.