Results 101 to 110 of about 2,247 (229)

Genetic alterations in craniosynostosis, genotype-phenotype correlations [PDF]

open access: yes, 2015
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  

Paediatric skull growth models: A systematic review of applications to normal skulls and craniosynostoses

open access: green, 2022
Maya Geoffroy   +3 more
openalex   +2 more sources

Advances in Craniofacial Surgery [PDF]

open access: yes, 2016
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
core   +1 more source

Staged dissection reduces blood loss in surgery for metopic synostosis

open access: yesJournal of Plastic Surgery and Hand Surgery
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
doaj   +1 more source

Long-term treatment results of craniosynostosis [PDF]

open access: yes
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
core   +1 more source

Correction of maxillofacial deformities in a patient with unilateral coronal craniosynostosis (plagiocephaly): a case report and a review of literatures.

open access: yesFrontiers in Dentistry, 2013
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]

open access: yes
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
core   +3 more sources

Zmieniające się cechy sonograficzne zespołu Aperta w diagnostyce prenatalnej – opis przypadku i przegląd literatury [PDF]

open access: yes, 1970
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
core   +1 more source

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