Results 11 to 20 of about 9,125 (154)

Ocular biometric features of pediatric patients with fibroblast growth factor receptor-related syndromic craniosynostosis

open access: yesScientific Reports, 2021
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
doaj   +1 more source

Surgical treatment and muscle protein analysis of V-pattern exotropia in craniosynostosis

open access: yesScientific Reports, 2022
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
doaj   +1 more source

Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?

open access: yesFrontiers in Pediatrics, 2021
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
doaj   +1 more source

Ophthalmological findings in children with non-syndromic craniosynostosis: preoperatively and postoperatively up to 12 months after surgery

open access: yesBMJ Open Ophthalmology, 2021
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
doaj   +1 more source

Prevalence of Cardiac Anomalies in Children with Syndromic and Non-syndromic Craniosynostosis [PDF]

open access: yesInternational Clinical Neuroscience Journal, 2022
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
doaj   +1 more source

High risk factors for craniosynostosis during pregnancy: A case-control study

open access: yesEuropean Journal of Obstetrics & Gynecology and Reproductive Biology: X, 2022
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
doaj   +1 more source

Craniosynostosis

open access: yesClinical Radiology, 2013
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

Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay

open access: yesFrontiers in Pediatrics, 2022
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
doaj   +1 more source

Comparison of Perioperative Anesthetic Concerns in Simple and Complex Craniosynostosis Cases: A Retrospective Study

open access: yesJournal of Neuroanaesthesiology and Critical Care, 2022
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
doaj   +1 more source

ERN CRANIO patient coverage of craniosynostosis in Europe

open access: yesOrphanet Journal of Rare Diseases, 2022
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

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