Results 11 to 20 of about 15,355 (176)

Craniosynostosis

open access: yesAdvances in Clinical Neuroscience & Rehabilitation, 2019
Craniosynostosis is a group of conditions characterised by the premature fusion of one or more cranial vault sutures. This may lead to abnormal cranial development with severe skull and craniofacial deformities and if the condition is left untreated ...
Josephine Jung   +4 more
doaj   +2 more sources

Impact of data synthesis strategies for the classification of craniosynostosis [PDF]

open access: yesFrontiers in Medical Technology, 2023
IntroductionPhotogrammetric surface scans provide a radiation-free option to assess and classify craniosynostosis. Due to the low prevalence of craniosynostosis and high patient restrictions, clinical data are rare.
Matthias Schaufelberger   +10 more
doaj   +2 more sources

Craniofacial Morphology and Dental Age Assessment in Pediatric Craniosynostosis: A Comparative Cross-Sectional Study. [PDF]

open access: yesClin Exp Dent Res
ABSTRACT Objectives To delineate the craniofacial morphometric characteristics of Thai children with syndromic (SC) and non‐syndromic craniosynostosis (NSC) and to assess dental maturation relative to Chronological Age (CA). Methods This comparative cross‐sectional study evaluated 19 patients (SC: n = 13; NSC: n = 6; mean age 9.32 ± 2.67 years ...
Ratanasereeprasert N   +7 more
europepmc   +2 more sources

When Virchow's law fails: Crouzon syndrome as a test case for quantitative suture closure-endocranial shape relationships. [PDF]

open access: yesJ Anat
Crouzon syndrome shows preserved intracranial volume but profoundly altered endocranial shape, with disrupted allometric coupling relative to controls. Treating calvarial suture patency as a continuous, age‐adjusted variable reveals strong system‐level covariation with endocranial morphology, effects invisible to conventional categorical suture scoring.
Steup FWR   +9 more
europepmc   +2 more sources

Craniosynostosis: To study the spectrum and outcome of surgical intervention at a tertiary referral institute in India

open access: yesJournal of Pediatric Neurosciences, 2020
Aims and Objectives: This study aimed to analyze the spectrum and surgical outcome of cases of craniosynostosis operated at a tertiary referral institute in IndiaDesign: This was a cross-sectional study. Materials and Methods: We retrospectively examined
Charandeep S Gandhoke   +4 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

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

Effects of Thyroxine Exposure on Osteogenesis in Mouse Calvarial Pre-Osteoblasts [PDF]

open access: yes, 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   +2 more sources

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

Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples

open access: yesFrontiers in Neuroscience, 2017
Craniosynostosis is a heterogeneous condition caused by the premature fusion of cranial sutures, occurring mostly as an isolated anomaly. Pathogenesis of non-syndromic forms of craniosynostosis is largely unknown.
Marcella Zollino   +7 more
doaj   +1 more source

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