Results 171 to 180 of about 18,979 (223)
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Elevated Intracranial Pressure in Patients with Craniosynostosis by Optical Coherence Tomography
Plastic and Reconstructive Surgery, 2022Background: Craniosynostosis may lead to elevated intracranial pressure, which may be implicated with impaired neurocognitive development. However, accurately measuring intracranial pressure is challenging, and patterns in craniosynostosis patients are ...
C. Kalmar +10 more
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Epidemiology, Genetics, and Pathophysiology of Craniosynostosis.
Oral and Maxillofacial Surgery Clinics of North America, 2022Craniosynostosis, the premature fusion of the infant cranial skulls, can be recognized by characteristic head shape differences that worsen with head growth. Craniosynostosis can be syndromic or nonsyndromic and can involve one suture or multiple sutures.
M. Blessing, E. Gallagher
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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
openaire +2 more sources
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
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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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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
openaire +2 more sources
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
openaire +2 more sources