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Craniosynostosis
Understanding and managing the condition: A practical guide for families
Craniosynostosis
Craniosynostosis is a condition where the bones of an infant’s skull fuse together too early. In most cases, surgery in the first year of life will effectively correct it and the child can go on to expect a typical life. For a minority, craniosynostosis is part of a syndrome, which is a lifelong condition. This practical guide explains how craniosynostosis develops and the evidence-based, best-practice treatments. It also includes the lived experience of families.
Author and Series Information
The writing of Craniosynostosis was led by Dr. Ruth Barta, MD, Craniofacial and Pediatric Plastic Surgeon at Gillette Children’s, a world-renowned center of excellence for the treatment of brain, bone, and movement conditions. Craniosynostosis is part of the Gillette Children’s Healthcare Series, a series of books for families who are looking for clear, comprehensive information. Health care professionals, educators, students, and extended family members will also benefit from reading Craniosynostosis.
Other Titles in the Series
• Idiopathic Scoliosis
• Spastic Hemiplegia–Unilateral Cerebral Palsy
• Spastic Quadriplegia–Bilateral Cerebral Palsy
• Spastic Diplegia–Bilateral Cerebral Palsy, second edition
• Epilepsy
• Spina Bifida
• Osteogenesis Imperfecta
• Scoliosis: Congenital, Neuromuscular, Syndromic, and Other Causes
