Results 221 to 230 of about 24,851 (250)
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World Journal of Surgery, 1989
AbstractCraniosynostosis affects approximately one infant out of one thousand. Increase of intracranial pressure and risks of functional problems are more frequent than previously thought, especially in single‐suture synostosis. Frontocranial remodeling will correct both functional and esthetic consequences of craniosynostosis.
D, Marchac, D, Renier
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AbstractCraniosynostosis affects approximately one infant out of one thousand. Increase of intracranial pressure and risks of functional problems are more frequent than previously thought, especially in single‐suture synostosis. Frontocranial remodeling will correct both functional and esthetic consequences of craniosynostosis.
D, Marchac, D, Renier
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Pediatric Neurology, 2015
Craniosynostosis is the premature fusion of one or more of the cranial sutures. About 8% of the patients have familial or syndromic forms of synostosis, and in the remainder it occurs as a spontaneous isolated defect. Familial craniosynostosis syndromes are typically transmitted as an autosomal dominant trait resulting in disruption of the fibroblast ...
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Craniosynostosis is the premature fusion of one or more of the cranial sutures. About 8% of the patients have familial or syndromic forms of synostosis, and in the remainder it occurs as a spontaneous isolated defect. Familial craniosynostosis syndromes are typically transmitted as an autosomal dominant trait resulting in disruption of the fibroblast ...
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Clinical Radiology, 2002
Craniosynostosis, caused by premature fusion of the sutures, may be syndromic or non-syndromic. Radiology has an important role to play in the assessment, management and follow-up of these patients. Initial investigations may often be undertaken within general radiology departments. An understanding of the terminology and recognition of the predictable
R I, Aviv, E, Rodger, C M, Hall
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Craniosynostosis, caused by premature fusion of the sutures, may be syndromic or non-syndromic. Radiology has an important role to play in the assessment, management and follow-up of these patients. Initial investigations may often be undertaken within general radiology departments. An understanding of the terminology and recognition of the predictable
R I, Aviv, E, Rodger, C M, Hall
openaire +2 more sources
Journal of Neurosurgery, 1975
✓ The authors review the embryopathology and clinical manifestations of craniosynostosis and analyze a series of 27 children. The operative procedure of linear craniectomy and immediate cranioplasty is described and evaluated. Since few children with craniosynostosis have neurological deficits that can be ascribed to the skull anomalies, surgery to ...
E L, Foltz, J D, Loeser
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✓ The authors review the embryopathology and clinical manifestations of craniosynostosis and analyze a series of 27 children. The operative procedure of linear craniectomy and immediate cranioplasty is described and evaluated. Since few children with craniosynostosis have neurological deficits that can be ascribed to the skull anomalies, surgery to ...
E L, Foltz, J D, Loeser
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Clinics in Plastic Surgery, 2019
Nonsyndromic craniosynostosis is significantly more common than syndromic craniosynostosis, affecting the sagittal, coronal, metopic, and lambdoid sutures in decreasing order of frequency. Nonsyndromic craniosynostosis is most frequently associated with only 1 fused suture, creating a predictable head shape. Repair of craniosynostosis is recommended to
Robert F, Dempsey +8 more
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Nonsyndromic craniosynostosis is significantly more common than syndromic craniosynostosis, affecting the sagittal, coronal, metopic, and lambdoid sutures in decreasing order of frequency. Nonsyndromic craniosynostosis is most frequently associated with only 1 fused suture, creating a predictable head shape. Repair of craniosynostosis is recommended to
Robert F, Dempsey +8 more
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Facial Plastic Surgery Clinics of North America, 2016
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and other associated abnormalities, such as carpal-pedal anomalies and cognitive function impairment. More than 150 syndromes are associated with craniosynostosis.
James C, Wang +2 more
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Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and other associated abnormalities, such as carpal-pedal anomalies and cognitive function impairment. More than 150 syndromes are associated with craniosynostosis.
James C, Wang +2 more
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Ugeskrift for Læger
In this review craniosynostosis is a condition characterized by the premature fusion of one or more cranial sutures, leading to abnormal skull development. It can occur as a non-syndromal condition or be associated with craniofacial syndromes and learning difficulties. The condition affects 1 in 1.300-2.500 newborns.
Mikkel Bundgaard, Skotting +3 more
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In this review craniosynostosis is a condition characterized by the premature fusion of one or more cranial sutures, leading to abnormal skull development. It can occur as a non-syndromal condition or be associated with craniofacial syndromes and learning difficulties. The condition affects 1 in 1.300-2.500 newborns.
Mikkel Bundgaard, Skotting +3 more
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Plastic and Reconstructive Surgery, 2011
Complex craniosynostoses (i.e., multisutural, nonsyndromic) are rare and present unique treatment challenges. The authors sought to assess long-term outcomes, including postsurgical growth and development, to develop evidence-based treatment algorithms.A retrospective review of all patients identified as having multiple sutural synostosis excluding ...
Marcin, Czerwinski +2 more
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Complex craniosynostoses (i.e., multisutural, nonsyndromic) are rare and present unique treatment challenges. The authors sought to assess long-term outcomes, including postsurgical growth and development, to develop evidence-based treatment algorithms.A retrospective review of all patients identified as having multiple sutural synostosis excluding ...
Marcin, Czerwinski +2 more
openaire +2 more sources
Clinics in Plastic Surgery, 2019
Management strategies for syndromic craniosynostosis patients require multidisciplinary subspecialty teams to provide optimal care for complex reconstructive approaches. The most common craniosynostosis syndromes include Apert (FGFR2), Crouzon (FGFR2), Muenke (FGFR3), Pfeiffer (FGFR1 and FGFR2), and Saethre-Chotzen (TWIST).
Rajendra, Sawh-Martinez +1 more
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Management strategies for syndromic craniosynostosis patients require multidisciplinary subspecialty teams to provide optimal care for complex reconstructive approaches. The most common craniosynostosis syndromes include Apert (FGFR2), Crouzon (FGFR2), Muenke (FGFR3), Pfeiffer (FGFR1 and FGFR2), and Saethre-Chotzen (TWIST).
Rajendra, Sawh-Martinez +1 more
openaire +2 more sources