combined with a significant reduction in IQ. Craniosynostosis occurs in one in 2000 births. Craniosynostosis is part of a syndrome in 15% to 40% of affected...

affected as well, similar to Crouzon syndrome and Pfeiffer syndrome. Craniosynostosis occurs when the fetal skull and facial bones fuse too soon in utero...

4 Craniosynostosis (nonsyndromic) 4 Craniosynostosis and dental anomalies Craniosynostosis-anal anomalies-porokeratosis syndrome Craniosynostosis-Dandy-Walker...

enough space for the growing brain, craniosynostosis results in increased intracranial pressure. Craniosynostosis is called simple when one suture is...

characterized by the premature fusion of certain bones of the skull (craniosynostosis), which affects the shape of the head and face. The syndrome includes...

Osteogenesis imperfecta (IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all...

abnormal bone development (e.g. craniosynostosis syndromes) and cancer. FGFR2 mutations are the cause of several craniosynostosis syndromes: Acrocephalosyndactyly...

and Dandy-Walker malformation. Hydrocephalus can also occur with craniosynostosis, being a constant feature of kleeblattschadel and frequently seen in...

disorder syndrome characterized by congenital heart defects, sagittal craniosynostosis, and severe developmental delay. The condition has been reported in...

Shprintzen–Goldberg syndrome is a congenital multiple-anomaly syndrome that has craniosynostosis, multiple abdominal hernias, cognitive impairment, and other skeletal...