Results 11 to 20 of about 9,125 (154)
Ametropia is reported as a common ophthalmic manifestation in craniosynostosis. We retrospectively compared childhood refractive error and ocular biometric features of fibroblast growth factor receptor (FGFR)-related syndromic craniosynostosis patients ...
Byung Joo Lee +3 more
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Surgical treatment and muscle protein analysis of V-pattern exotropia in craniosynostosis
The purpose of this study was to compare the differences of V-pattern exotropia in craniosynostosis and normal children. 39 children were included in this study, 19 craniosynostosis and 20 children in control group.
Qingyu Liu +6 more
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Congenital diaphragmatic hernia (CDH) is a life-threatening birth defect that presents as either an isolated diaphragm defect or as part of a complex disorder with a wide array of anomalies (complex CDH).
Linda Gaillard +9 more
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Aims Craniosynostosis is a congenital condition characterised by premature fusion of one or more cranial sutures. The aim of this study was to analyse ophthalmic function before and after cranial surgery, in children with various types of non-syndromic ...
Gerd Holmström +3 more
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Prevalence of Cardiac Anomalies in Children with Syndromic and Non-syndromic Craniosynostosis [PDF]
Background: Craniosynostosis mostly occurs as a single abnormality; however, it may rarely occur concomitantly with other congenital abnormalities known as syndromic craniosynostosis.
Ali Riazi +7 more
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High risk factors for craniosynostosis during pregnancy: A case-control study
Background: Craniosynostosis is a birth defect involving premature cranial sutures’ fusion with an increasing prevalence and unknown underlying causes in nearly 80% of cases.
Sotirios Plakas +3 more
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Craniosynostosis is a complex condition, characterized by the premature fusion of one of more of the cranial sutures. They can be seen individually or as part of multisystem syndromes. This review uses computed tomography (CT) with three-dimensional reconstructions to help describe some of the types and classifications of craniosynostosis, as well as ...
S, Nagaraja, P, Anslow, B, Winter
+7 more sources
Craniosynostosis is a premature fusion of cranial sutures, resulting in abnormally shaped skull and brain development disorder. The description of craniosynostosis in patients with BCL11B mutations is rare.
Xuemei Zhao +10 more
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Background We compared intraoperative and postoperative anesthetic parameters between simple (S-single suture) and complex (C-more than one suture) craniosynostosis cases. Materials and Methods Data was collected from a retrospective review of
Gokuldas Menon +7 more
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ERN CRANIO patient coverage of craniosynostosis in Europe
Background Against the backdrop of the European Directive on patients’ rights in cross-border healthcare, 24 European Reference Networks (ERNs) were launched in 2017.
O. Spivack +2 more
doaj +1 more source

