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ObjectiveBeyond aesthetic implications, craniosynostosis can profoundly impact neurocognitive development. There is a notable gap in standardized methodologies for identifying which of these patients are at-risk for developing adverse neuropsychosocial outcomes through screening techniques. This research aims to identify and recommend a standardized, routine approach inclusive of free or low-cost screening instruments for patients with craniosynostosis that are easily administered in clinic with or without a trained examiner.DesignA systematic review was conducted. Data related to various developmental assessments were extracted and subsequently reviewed by two trained neuropsychologists for analysis, categorization, and recommendation.Main Outcomes MeasuresNeurocognitive screening assessments for patients with craniosynostosis.ResultsIn total, 114 different tests regarding neurocognitive examination of patients with craniosynostosis were cited. We identified six areas of neuropsychosocial development that are relevant for routine screening: Development, Social-Emotional/Behavioral, Adaptive Functioning, Academic Achievement, Autism, and ADHD/Attention. Within each category, screening recommendations are made, including instruments that are free or low-cost and can be easily administered in clinic with or without a trained examiner.ConclusionsLiterature supports the impact of craniosynostosis on neuropsychosocial development, so we urge teams to screen patients from an early age using these suggestions as they are free or relatively low-cost, can be administered to a wide range of patient ages, and can be administered in clinic with or without a trained examiner. This study serves as a starting point towards a more standardized approach to effectively evaluate and address the neurocognitive implications of craniosynostosis, ultimately enhancing patient care and treatment outcomes.
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http://dx.doi.org/10.1177/10556656251335475 | DOI Listing |
Craniosynostosis (CS), the premature fusion of 1 or more cranial sutures, can present with coexisting deformation plagiocephaly or brachiocephaly. While surgical correction is the standard for CS, the management of cases with concurrent positional head shape deformities remains undefined. This study aims to describe clinical outcomes in this subset of patients and evaluate the role of adjunct orthotic therapy in their management.
View Article and Find Full Text PDFAuris Nasus Larynx
September 2025
Department of Otolaryngology-Head and Neck Surgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
A cartilage-conduction hearing aid (CCHA) transmits sound vibrations to the inner ear via the ear cartilage rather than through air or bone. They can be used in patients with meatal atresia and persistent otorrhea. Unlike bone-conduction hearing aid (BCHA), there is no need for pressure between the transducer and the temporal bone.
View Article and Find Full Text PDFCureus
July 2025
Anesthesiology, University of Texas Medical Branch, Galveston, USA.
Hypervolemic hemodilution (HVH) is a blood-sparing technique increasingly used in pediatric neuroanesthesiology, particularly during high-risk procedures such as craniosynostosis repair. By expanding intravascular volume with crystalloids or colloids before surgery, HVH dilutes red blood cell concentration, thereby reducing their loss due to bleeding, while maintaining cerebral oxygenation and hemodynamic stability. This approach is especially valuable in pediatric patients, who are more susceptible to transfusion-related complications due to their limited blood volume and immature immune systems.
View Article and Find Full Text PDFBone Rep
September 2025
Department of Clinical Chemistry, and Department of Biomedical and Clinical Sciences, Linköping University, SE-58185 Linköping, Sweden.
Hypophosphatasia (HPP) is a rare inborn-error-of-metabolism caused by mutations in the gene, resulting in deficient activity of tissue-nonspecific alkaline phosphatase and impaired skeletal mineralization. Affected individuals have a higher prevalence of chronic kidney disease (CKD) than the general population. We report a woman who underwent craniosynostosis surgery in infancy and lost her deciduous teeth prematurely.
View Article and Find Full Text PDFJ Craniofac Surg
September 2025
Division of Plastic Surgery, Children's Hospital Colorado.
Introduction: Fronto-orbital advancement (FOA) is the standard treatment for craniosynostosis patients with fronto-orbital dysmorphology. Few studies examine the incidence of secondary cranioplasty operations after FOA. This retrospective analysis utilizes multicenter billing data to identify risk factors and the incidence of secondary reconstructive cranioplasty operations after FOA.
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