Results 131 to 140 of about 9,125 (154)
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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
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Craniosynostosis and hydrocephalus
Neurosurgery, 1987Abstract Ten cases of craniosynostosis associated with hydrocephalus were found in a retrospective review of 250 cases of children with craniosynostosis. Four children had Pfeiffer's syndrome, 3 had Crouzon's syndrome, 2 had kleeblattschädel with multiple anomalies and therefore could not be classified into a definite syndrome, and 1 had
M, Golabi, M S, Edwards, D K, Ousterhout
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Benchmarking for Craniosynostosis
Journal of Craniofacial Surgery, 2007The quality of care for craniofacial malformations is thought to be improved through benchmarking. The benchmarking process identifies the best practice within the participating centers and leads to new protocols and guidelines, which are implemented by the participants. It also allows for comparison of outcome between the various centers.
Mathijssen, Irene, Arnaud, E
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Pediatrics In Review, 1995
On the surface, premature closure of one or more sutures of the skull may appear to be a straightforward malformation that leads to a specific, recognizable pattern of symptoms and signs, an anomaly that can be corrected simply by a surgical procedure. But in fact, craniosynostosis, which occurs in approximately I in 2500 children, is a dynamic process,
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On the surface, premature closure of one or more sutures of the skull may appear to be a straightforward malformation that leads to a specific, recognizable pattern of symptoms and signs, an anomaly that can be corrected simply by a surgical procedure. But in fact, craniosynostosis, which occurs in approximately I in 2500 children, is a dynamic process,
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Neonatal Network, 2009
Craniosynostosis is characterized by the fusion of sutures. It presents with an abnormal head shape. This article examines this defect and discusses its embryologic origin. A systemic physical assessment guide serves as a tool to enhance early recognition of this defect. Pictorial examples increase understanding of the defect. A discussion of treatment
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Craniosynostosis is characterized by the fusion of sutures. It presents with an abnormal head shape. This article examines this defect and discusses its embryologic origin. A systemic physical assessment guide serves as a tool to enhance early recognition of this defect. Pictorial examples increase understanding of the defect. A discussion of treatment
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American family physician, 2004
Skull deformity in infants continues to be a diagnostic and therapeutic challenge. Deformational plagiocephaly is a common and somewhat benign cause of skull deformity in infants that must be distinguished from the more serious craniosynostosis, which occurs alone or as a syndrome.
Haidar, Kabbani, Talkad S, Raghuveer
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Skull deformity in infants continues to be a diagnostic and therapeutic challenge. Deformational plagiocephaly is a common and somewhat benign cause of skull deformity in infants that must be distinguished from the more serious craniosynostosis, which occurs alone or as a syndrome.
Haidar, Kabbani, Talkad S, Raghuveer
openaire +1 more source