Syndromic craniosynostosis encompasses an array of diagnoses and genetic mutations that
affect the cranial vault, with additional anomalies in embryologically distinct anatomic sites …

The management of craniosynostosis, especially in the setting of craniofacial syndromes, is
ideally done in a multidisciplinary clinic with a team focused toward comprehensive care …

Crouzon, Apert, Pfeiffer, Muenke, and Saethre-Chotzen syndromes are the five most
common forms of syndromic craniosynostosis. Although each has different genetic …

OBJECT The authors present a retrospective cohort study examining complications in
patients undergoing surgery for craniosynostosis using both minimally invasive endoscopic …

Background: The authors hypothesize that early posterior vault distraction osteogenesis
safely confers considerable cranial vault remodeling, sufficient to enable fronto-orbital …

Background: The cephalic index is often used to evaluate sagittal craniosynostosis
corrections; however, validation of this measure remains untested. Methods: A three-part …

Purpose Craniosynostosis, which describes premature fusion of one or more cranial sutures,
has been associated with a variety of neurocognitive deficits. We sought to explore the …

OBJECTIVE The authors sought to evaluate the accuracy of a novel telehealth-compatible
diagnostic software system for identifying craniosynostosis within a newborn (< 1 year old) …

Background: Distraction osteogenesis has been proposed as an alternative to cranial
remodeling surgery for craniosynostosis, but technique descriptions and outcome analyses …

A persistent abnormal head shape is a concerning finding in an infant and can be from
craniosynostosis (intrinsic) or deformational plagiocephaly (DP; extrinsic) causes. It is …