Results 21 to 30 of about 13,286 (221)
BMJ 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
High risk factors for craniosynostosis during pregnancy: A case-control study
European 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
Prevalence of Cardiac Anomalies in Children with Syndromic and Non-syndromic Craniosynostosis [PDF]
International 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
Neuropsychological outcomes and health-related quality of life of children operated for nonsyndromic craniosynostosis [PDF]
, 2021 The primary aim of this thesis was to assess the intelligence quotient, attention function, adaptive behavior skills, and health-related quality of life of children operated for nonsyndromic craniosynostosis.
Kljajic, Marizela
core +1 more source
Frontiers 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
Journal 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
Clinical 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
openaire +5 more sources
Effects of Thyroxine Exposure on Osteogenesis in Mouse Calvarial Pre-Osteoblasts [PDF]
, 2013 The incidence of craniosynostosis is one in every 1,800-2500 births. The gene-environment model proposes that if a genetic predisposition is coupled with environmental exposures, the effects can be multiplicative resulting in severely abnormal phenotypes.
Mohammed Elsalanty +19 more
core +1 more source
ERN CRANIO patient coverage of craniosynostosis in Europe
Orphanet 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
Hydrocephalus and craniosynostosis [PDF]
Neurosurgical Focus, 1997 Object A retrospective study of 1727 cases of craniosynostosis was undertaken to determine the interrelationship between abnormal cerebrospinal fluid (CSF) hydrodynamics and craniosynostosis. Methods The patients were divided intwo two
G, Cinalli +9 more
openaire +2 more sources