Results 101 to 110 of about 2,247 (229)
Book Review: The Craniosynostoses: Causes, Natural History and Management [PDF]
Farhad Afshar
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Genetic alterations in craniosynostosis, genotype-phenotype correlations [PDF]
A koponyavarratok idő előtti fúziójának következtében kialakuló craniosynostosis klinikailag és etiológiailag heterogén betegségcsoport. A betegek többségére jellemző izolált (nem-szindrómás) forma kialakulásában a környezeti és a genetikai faktorok ...
Bessenyei, Beáta
core
Advances in Craniofacial Surgery [PDF]
Calvaria development initiates by growth from primary ossification centers meeting each other to form suture sites. The term craniosynostosis describes premature fusion of one or more of the calvarial sutures.
Hashemi, Hamid Mahmoud +2 more
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Staged dissection reduces blood loss in surgery for metopic synostosis
INTRODUCTION: Fronto-orbital remodelling for metopic synostosis is an extensive operation with substantial blood loss, particularly from emissary veins in the glabellar region.
Anna Sundelin +8 more
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Long-term treatment results of craniosynostosis [PDF]
Craniosynostosis patients experience multiple problems due to improper growth of the skull. The purpose of this study was to evaluate the long-term treatment results of patients operated on for sagittal or metopic synostosis in a single centre study.
Svalina, Anja
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Plagiocephaly (oblique skull) is premature fusion of one of the coronal sutures. Frontal plagiocephaly is a rare congenital deformity in the skull that is the most complicated form of craniosynostosis to treat. Examination of all sutures is necessary for
Mansour Khorasani +2 more
doaj
AI-based diagnosis and phenotype – Genotype correlations in syndromic craniosynostoses [PDF]
Apert (AS), Crouzon (CS), Muenke (MS), Pfeiffer (PS), and Saethre Chotzen (SCS) are among the most frequently diagnosed syndromic craniosynostoses. The aims of this study were (1) to train an innovative model using artificial intelligence (AI)–based ...
Amiel, Jeanne +19 more
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Zmieniające się cechy sonograficzne zespołu Aperta w diagnostyce prenatalnej – opis przypadku i przegląd literatury [PDF]
Apert syndrome is characterized by craniosynostosis, midfacial malformations and symmetrical syndactyly of the hands and feet. We report a case of prenatal sonographic diagnosis of Apert syndrome.
Respondek-Liberska, Maria +3 more
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The Craniosynostoses: Causes, Natural History and Management. [PDF]
Farhad Afshar
openalex +2 more sources

