Zobrazeno 1 - 10
of 15 149
pro vyhledávání: '"craniosynostosis"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract This study constructed deep learning models using plain skull radiograph images to predict the accurate postnatal age of infants under 12 months. Utilizing the results of the trained deep learning models, it aimed to evaluate the feasibility
Externí odkaz:
https://doaj.org/article/41e2f19569c3412b9db51a398c4de114
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Kevin Bloch, Maya Geoffroy, Maxime Taverne, Lara van de Lande, Eimear O’Sullivan, Ce Liang, Giovanna Paternoster, Mehran Moazen, Sébastien Laporte, Roman Hossein Khonsari
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Trigonocephaly occurs due to the premature fusion of the metopic suture, leading to a triangular forehead and hypotelorism. This condition often requires surgical correction for morphological and functional indications. Metopic ri
Externí odkaz:
https://doaj.org/article/d7d89885186043d6851b03b72c004147
Autor:
Anthony M. Musolf, Cristina M. Justice, Zeynep Erdogan-Yildirim, Seppe Goovaerts, Araceli Cuellar, John R. Shaffer, Mary L. Marazita, Peter Claes, Seth M. Weinberg, Jae Li, Craig Senders, Marike Zwienenberg, Emil Simeonov, Radka Kaneva, Tony Roscioli, Lorena Di Pietro, Marta Barba, Wanda Lattanzi, Michael L. Cunningham, Paul A. Romitti, Simeon A. Boyadjiev
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Craniosynostosis (CS) is a major birth defect resulting from premature fusion of cranial sutures. Nonsyndromic CS occurs more frequently than syndromic CS, with sagittal nonsyndromic craniosynostosis (sNCS) presenting as the most common CS p
Externí odkaz:
https://doaj.org/article/f648374bc2b0416ab9f8c6846eee6350
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-6 (2024)
Abstract Background Functional and structural complexities associated with craniosynostosis present challenges for families of affected individuals. Additionally, these patients undergo childhood surgeries that significantly impact the role of the fa
Externí odkaz:
https://doaj.org/article/695809c130234c6bb9af4aff532f5599
Autor:
Attill Saemann, Sina Schmid, Maria Licci, Marek Zelechowski, Balazs Faludi, Philippe C. Cattin, Jehuda Soleman, Raphael Guzman
Publikováno v:
Frontiers in Surgery, Vol 11 (2024)
BackgroundCraniosynostosis is a type of skull deformity caused by premature ossification of cranial sutures in children. Given its variability and anatomical complexity, three-dimensional visualization is crucial for effective teaching and understand
Externí odkaz:
https://doaj.org/article/118a134e0cb14ae8846baf0ef54d4def
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background and objective The pathogenesis of coronal suture craniosynostosis is often attributed to the dysregulated cellular dynamics, particularly the excessive proliferation and abnormal osteogenic differentiation of suture cells. Despite
Externí odkaz:
https://doaj.org/article/ca15c9ae5b8248c0aba7ec0032342030
Autor:
Neeharika P Shah, Omkar N Gadre
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 62, Iss 1, Pp 117-120 (2024)
Craniosynostoses are syndromes characterized by premature fusion of sutures of the skull and Crouzon syndrome is the most common of the craniosynostosis syndromes. Early fusion of sutures causes craniofacial anomalies. Visual complications can arise-
Externí odkaz:
https://doaj.org/article/f20bb0d8e4234636aa87645e8658b89a