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...

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

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

Cole-Carpenter syndrome 2 Craniorhiny Craniosynostosis (nonsyndromic) 6 Craniosynostosis, Boston-type (nonsyndromic) Craniosynostosis and dental anomalies Fontaine...

can grow. Premature complete ossification of the sutures is called craniosynostosis. After infancy, the anterior fontanelle is known as the bregma. An...

Muenke syndrome, also known as FGFR3-related craniosynostosis, is a human specific condition characterized by the premature closure of certain bones of...

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...