Craniosynostosis is a major congenital craniofacial disorder characterized by the premature
fusion of cranial suture (s). Patients with severe craniosynostosis often have impairments in …

Introduction One third of patients with craniofacial dysostosis syndromes and about 15–20%
of children with single suture craniostenosis have a documented increase in intracranial …

This guideline for care of children with craniosynostosis was developed by a national
working group with representatives of 11 matrix societies of specialties and the national …

Background: The relationship between surgical age and long-term neuropsychological
outcomes in sagittal-suture craniosynostosis remains equivocal. Whole-vault cranioplasty …

Craniosynostosis is a defect of the skull caused by early fusion of one or more of the cranial
sutures and affects 3 to 5 individuals per 10,000 live births. Craniosynostosis can be divided …

Apert syndrome is a distinctive human malformation characterized by craniosynostosis and
severe syndactyly of the hands and feet. It is caused by specific missense substitutions …

Although most cases of craniosynostosis are nonsyndromic, craniosynostosis is known to
occur in conjunction with other anomalies in well-defined patterns that make up clinically …

Craniosynostosis, the premature ossification of one or more skull sutures, is a clinically and
genetically heterogeneous congenital anomaly affecting approximately one in 2,500 live …

Nonsyndromic craniosynostosis is significantly more common than syndromic
craniosynostosis, affecting the sagittal, coronal, metopic, and lambdoid sutures in …

Object. In this study the authors investigated whether patterns of intracranial venous
drainage in children with complex craniosynostosis associated with raised intracranial …