Results 11 to 20 of about 13,286 (221)

Difference in anterior fontanelle closure between non-syndromic craniosynostosis and normal controls: a retrospective cross-sectional study [PDF]

Italian Journal of Pediatrics
Background This study aimed to investigate the differences in anterior fontanelle closure time and size between children with non-syndromic craniosynostosis and controls on CT imaging. Methods A retrospective cross-sectional study was conducted involving
Jinhua Fu, Qijia Zhan, Jiangang Liu, Rui Zhao, Wenbin Jiang   +4 more
doaj   +2 more sources

Neurocognitive outcomes of children with non-syndromic single-suture craniosynostosis

Child's Nervous System, 2022
While the focus of craniosynostosis surgery is to improve head shape, neurocognitive sequelae are common and are incompletely understood. Neurodevelopmental problems that children with craniosynostosis face include cognitive and language impairments ...
Christopher L Kálmár, Shih-Shan Lang, Gregory G Heuer   +2 more
exaly   +1 more source

MSC Membrane‐Coated circPROSC‐siRNA Nanoparticles for Ameliorating Craniosynostosis by Inhibiting Premature Suture Ossification [PDF]

Advanced Science
Craniosynostosis is a congenital craniofacial disorder caused by excessive osteogenic differentiation of mesenchymal stem cells (MSCs) within cranial sutures.
Zhenkun Weng, Xiu Chen, Jin Xu, Qing Yan, Jian Jiao, Qian Liu, Aihua Gu   +6 more
doaj   +2 more sources

Evaluation and management of nonsyndromic craniosynostosis

Acta Paediatrica, International Journal of Paediatrics, 2011
Craniosynostosis (craniostenosis) is premature fusion of the sutures of the cranial vault. Several factors can affect the growth of the cranial vault during embryonic life and after birth, leading to different types of craniosynostosis; these can be ...
Laura Papetti, Mario Pagnoni, F Nicita   +2 more
exaly   +2 more sources

Apert Syndrome: A Case Report [PDF]

Iranian Journal of Neonatology, 2022
Background: Primary craniosynostosis is a form of premature fusion of the cranial sutures, which commonly occurs prenatally. The condition appears in both syndromic and nonsyndromic forms.Case report: The cause of most cases of primary craniosynostosis ...
Shahin Mafinejad, Hojat Ehteshammanesh, Ghasem Bayani, Hosein Mahmoodzade   +3 more
doaj   +1 more source

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, Mark Urata, Jian-Fu Chen, Yang Chai   +3 more
doaj   +1 more source

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
Craig F Munns, Edward P Maguire, Angela Williams, Sue Wood, Andrew Biggin   +4 more
doaj   +1 more source

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

Scientific 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, Kihwang Lee, Seung Ah Chung, Hyun Taek Lim   +3 more
doaj   +1 more source

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

Scientific 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, Yuan Li, Siying Wang, Wenjing Zheng, Han Ye, Wen Li, Tong Qiao   +6 more
doaj   +1 more source

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

Frontiers 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, Anne Goverde, Quincy C. C. van den Bosch, Fernanda S. Jehee, Erwin Brosens, Danielle Veenma, Frank Magielsen, Annelies de Klein, Irene M. J. Mathijssen, Marieke F. van Dooren   +9 more
doaj   +1 more source