Results 11 to 20 of about 18,979 (223)
Neuro-Ophthalmological Manifestations of Craniosynostosis: Current Perspectives
Eye and Brain, 2021 Craniosynostosis, a premature fusion of cranial sutures that can be isolated or syndromic, is a congenital defect with a broad, multisystem clinical spectrum.
Jesse Skoch, Brian Pan
exaly +4 more sources
The clinical manifestations, molecular mechanisms and treatment of craniosynostosis
Disease Models & Mechanisms, 2022 Craniosynostosis is a major congenital craniofacial disorder characterized by the premature fusion of cranial suture(s). Patients with severe craniosynostosis often have impairments in hearing, vision, intracranial pressure and/or neurocognitive ...
Eloise Stanton +3 more
semanticscholar +3 more sources
Craniosynostosis in Patients With X‐Linked Hypophosphatemia: A Review
JBMR Plus, 2023 Craniosynostosis is a rare condition of skull development, manifesting during fetal and early infant development, and is usually congenital. Craniosynostosis secondary to metabolic disorders, such as X‐linked hypophosphatemia (XLH), is less common and is
C. Munns +4 more
semanticscholar +2 more sources
The Journal of Clinical Investigation, 2023 Skull development coincides with the onset of cerebrospinal fluid (CSF) circulation, brain-CSF perfusion, and meningeal lymphangiogenesis, processes essential for brain waste clearance.
Matt J. Matrongolo +9 more
semanticscholar +3 more sources
A Radiation-Free Classification Pipeline for Craniosynostosis Using Statistical Shape Modeling
Diagnostics, 2022 Background: Craniosynostosis is a condition caused by the premature fusion of skull sutures, leading to irregular growth patterns of the head. Three-dimensional photogrammetry is a radiation-free alternative to the diagnosis using computed tomography ...
Matthias Schaufelberger +10 more
semanticscholar +3 more sources
Prevalence of Ocular Anomalies in Craniosynostosis: A Systematic Review and Meta-Analysis
Journal of Clinical Medicine, 2022 Background: The aim of this study was to describe the ophthalmic abnormalities and their prevalence in craniosynostosis prior to craniofacial surgery. Methods: A systematic search was conducted on Medline OVID, Embase, Cochrane, Google Scholar, Web of ...
, Parinaz Rostamzad, Maarten Koudstaal
exaly +2 more sources
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 ...
E. Ntoula +3 more
semanticscholar +3 more sources
Advances in Clinical Neuroscience & Rehabilitation, 2019 Craniosynostosis is a condition of one or more of the fibrous sutures in an infant skull prematurely fuses by turning into bone (ossification). 1 Premature fusion of cranial sutures may have an effect on cranial shape an less frequently on brain growth ...
Manish Pandya +4 more
semanticscholar +3 more sources
Nonsyndromic Craniosynostosis [PDF]
Seminars in Plastic Surgery, 2012 Nonsyndromic craniosynostosis is more commonly encountered than syndromic cases in pediatric craniofacial surgery. Affected children display characteristic phenotypes according to the suture or sutures involved. Restricted normal growth of the skull can lead to increased intracranial pressure and changes in brain morphology, which in turn may ...
Rohit Khosla
exaly +3 more sources
Syndromic Craniosynostosis [PDF]
Seminars in Plastic Surgery, 2012 Although most cases of craniosynostosis are nonsyndromic, craniosynostosis is known to occur in conjunction with other anomalies in well-defined patterns that make up clinically recognized syndromes. Patients with syndromic craniosynostoses are much more complicated to care for, requiring a multidisciplinary approach to address all of their needs ...
Christopher Derderian
exaly +3 more sources