Results 11 to 20 of about 24,851 (250)

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

Ophthalmological findings in children with non-syndromic craniosynostosis: preoperatively and postoperatively up to 12 months after surgery

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, Eva Larsson, Evangelia Ntoula, Daniel Nowinski   +3 more
doaj   +1 more source

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.
A Mansukhani, AK Coussens, BD Stamper, BK Huang, BU Ang, C Owen, C Yao, CB Harvey, CH Shackleton, CW Li, D Gomez, D Johnson, DC Robinson, DP Rice, DT Gault, G Radetti, G Ramajayam, GA Brent, GM Morriss-Kay, GR Williams, H Kohara, H Miraoui, HJ Kim, J Connerney, J Esparza, J Zumbrunn, JA Greenwald, Jack C. Yu, James J. Cray, JH Bassett, JH Oh, JL Penfold, JM Britto, JQ Feng, JS Morey, K Kasono, KA Kapp-Simon, Kameron Khaksarfard, KM Lee, M Bodo, M Menking, M Segni, MH Sheng, MM Cohen Jr, Mohammed Elsalanty, PJ Marie, R Rice, S Akita, S Wadhwa, S Weiss, SA Boyadjiev, SA Rasmussen, Seth M. Weinberg, W Arlt, W Riggs Jr, WM Chadduck, Xing-Ming Shi, Y Xiong, Z von Marschall   +58 more
core   +7 more sources

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, Evangelos Anagnostou, Angelos Christos Plakas, Maria Piagkou   +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, Mahdi Vahidian, Mehrdad Larry, Donya Sheibani Tehrani, Mostafa Alami, Zahra Salehi, Maryam Karimi, Sarina Loghmani   +7 more
doaj   +1 more source

Craniosynostosis

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
  +7 more sources

Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay

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, Bingbing Wu, Huiyao Chen, Ping Zhang, Yanyan Qian, Xiaomin Peng, Xinran Dong, Yaqiong Wang, Gang Li, Chenbin Dong, Huijun Wang   +10 more
doaj   +1 more source