Results 181 to 190 of about 13,286 (221)
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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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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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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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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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American Journal of Medical Genetics, 2000
Cherubism is a rare autosomal dominant fibro-osseous disorder that affects almost exclusively maxilla and mandible. Extracranial skeletal involvement is rare. We report on three affected males in three generations. The youngest affected relative was examined at age 4 months. He also had craniosynostosis.
M, Stiller +7 more
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Cherubism is a rare autosomal dominant fibro-osseous disorder that affects almost exclusively maxilla and mandible. Extracranial skeletal involvement is rare. We report on three affected males in three generations. The youngest affected relative was examined at age 4 months. He also had craniosynostosis.
M, Stiller +7 more
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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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Journal of Neurosurgery, 1970
✓ In 25 Egyptian patients 2 to 18 years of age, craniosynostosis was studied clinically, radiologically, and biochemically. Oxycephaly was the most common manifestation, but single suture synostosis occurred occasionally. Increased intracranial pressure was marked (76%), clinically, radiologically, and at operation.
H, el-Sherif +3 more
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✓ In 25 Egyptian patients 2 to 18 years of age, craniosynostosis was studied clinically, radiologically, and biochemically. Oxycephaly was the most common manifestation, but single suture synostosis occurred occasionally. Increased intracranial pressure was marked (76%), clinically, radiologically, and at operation.
H, el-Sherif +3 more
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Strabismus in Craniosynostosis
Journal of Pediatric Ophthalmology & Strabismus, 2013Strabismus is common in craniosynostosis, with rates from 39% to 90.9% in Crouzon, Apert, Pfeiffer, and Saethre-Chotzen syndromes. This article reviews the epidemiology of strabismus in these disorders and discusses competing theories of the mechanism, including absent muscles, excyclorotation of muscles, and instability of muscle pulleys.
Jamie B, Rosenberg +2 more
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Hydrocephalus in craniosynostosis
Child's Nervous System, 1988Routine CT scanning in 221 patients with craniosynostosis revealed ventricular dilation in 40. In 5 hydrocephalus was obviously unrelated to the craniostenosis. The remaining 35 cases were associated almost exclusively with syndromic craniosynostosis. Ventricular dilation was mild in 22, moderate in 9, and marked in 4 patients.
H, Collmann +3 more
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Genetic perspectives on craniosynostosis and syndromes with craniosynostosis
Journal of Neurosurgery, 1977✓ Thirty-seven syndromes in which craniosynostosis is a feature are presented in tabular form, allowing the clinician to rapidly identify a given syndrome and gain immediate access to the pertinent literature. A plea is made to delineate unknown genesis syndromes with craniosynostosis as rapidly as possible.
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