Apert syndrome is a genetic disorder, characterized by deformities of the skull, face, and limbs affecting an individual’s health, daily function, and social interaction. Successful treatment of …

With the present work we emphasize the need of an integrated and multispecialistic approach to the syndrome. We want to define main therapeutic steps performed by our group on patients …

To reach these goals, we adopted endoscopy-assisted craniosynostosis surgery (EACS) supplemented with helmet molding therapy in 2005. We present in detail our surgical …

lowed by helmet therapy, we can significantly reduce the skull shape deformity in children with Apert syndrome. More importantly, our center advocates for an early endoscopic suture …

Screen every 6 months with Apert syndrome, Saethre-Chotzen, and multisuture craniosynostosis, and every year for Muenke syndrome. The treatment of ICP depends on the causative factors …

Apert syndrome is a rare genetic disorder characterized by distinct physical features that intricately touch the skull, face, hands, and feet. While there is currently no cure for Apert …

Helmet therapy After minimally invasive surgery, office visits at certain intervals are needed to fit a series of helmets to help shape your baby's skull. The surgeon will determine the length of …

Nov 22, 2021 · Apert syndrome is a rare condition caused by a genetic mutation that occurs early during pregnancy. The mutation could be inherited or newly formed (de novo). There is a 50% …

Children with Apert Syndrome benefit from routine psychosocial support to address any behavioral, developmental, academic, emotional or social difficulties associated with their …

Awareness of potential airway compromise & proactive airway mgmt are crucial in infants & children. Specific airway mgmt in Apert syndrome will depend on level & severity of …