Results 61 to 70 of about 3,158 (217)
CRANIOFACIAL RECONSTRUCTIONS IN CHILDREN WITH CRANIOSYNOSTOSIS
Slovenska pediatrija, 2021 Background. Craniosynostosis is a group of rare congeni-tal diseases of the skull. They arise from premature ossification of one or more cranial sutures. This represents an obstruction to normal brain growth and leads to specific deformations of the skull,
Peter Spazzapan +3 more
doaj +1 more source
Acta Ophthalmologica, Volume 102, Issue 5, Page 564-572, August 2024.Abstract Purpose To evaluate the refractive outcome and strabismus at 5 years of age, in children operated for various types of non‐syndromic craniosynostosis, and further analyse the refractive and strabismic development over time. Methods Eighty‐nine children, who had undergone operations for non‐syndromic craniosynostosis, were examined at 5 years ...
Evangelia Ntoula +3 more
wiley +1 more source
Crouzons syndrome: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2007 Human skull is made up of many bone joints connected by sutures. The sutures fuse in later life after the complete growth of the brain. If any of these sutures closes early, it may interfere with the normal growth of the brain.
Arathi R, Sagtani A, Baliga M
doaj
Congenital malformations [PDF]
, 2012 Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or during the intrauterine life. Their global birth prevalence is about 2–3%.
CORSELLO, Giovanni, GIUFFRE, Mario
core +1 more source
Pycnodysostosis: Characteristics of teeth, mouth and jaws
Orthodontics &Craniofacial Research, Volume 27, Issue 4, Page 656-664, August 2024.Abstract Objectives To describe the clinical and radiographic oro‐dental characteristics of patients with pycnodysostosis (PDO). Materials & Methods A short interview and clinical examination of seven patients with PDO were performed as well as assessment of the temporomandibular joints and masticatory muscles using the diagnostic criteria for ...
Nikolaos Ferlias +3 more
wiley +1 more source
Premature Craniosynostosis in a Rare Genetic Disease- A Case Report
Iranian Journal of Public Health, 2015 Background: Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity.Its most notable characteristic feature is premature synostosis of cranial sutures .The case presented is ...
Hasnain Abbas Dharamshi +6 more
doaj
Sagittal craniosynostosis combined with ossified cephalhematoma—a tricky and demanding puzzle [PDF]
, 2018 Introduction: Four cases of sagittal synostosis combined with ossified cephalhematoma prompted the authors to present the data and to discuss the implications.
Kaiser, Georges, Oesch, Valérie
core
General and oral aspects in Apert syndrome: report of a case [PDF]
, 2015 Background: The present paper describes the general and oral manifestations in a 32-year-old man previously diagnosed with Apert syndrome. Clinical examination revealed features of acrocephalosyndactyly.
Chimenos Küstner, Eduardo +5 more
core +1 more source
Advanced Theory and Simulations, Volume 7, Issue 7, July 2024.Sagittal synostosis is the most common type of craniosynostosis. Spring‐assisted cranioplasty is a minimally invasive technique used to correct sagittal synostosis. The surgical outcome in spring‐assisted cranioplasty depends on multiple factors. Results of this study show that elastic modulus of the bones and bone thickness have significant effects on
Jenson Jacob, Selim Bozkurt
wiley +1 more source
Revista Brasileira de Cirurgia Plástica, 2011 INTRODUÇÃO: A craniossinostose coronal unilateral (CCU) é a ossificação prematura da sutura coronal unilateralmente e provoca uma deformidade em 3 dimensões, que pode afetar o crânio e as órbitas.
Cassio Eduardo Raposo-do-Amaral +5 more
doaj +1 more source