Results 11 to 20 of about 5,138 (198)

Prevalence and Patterns of Permanent Tooth Agenesis in Patients With Crouzon or Apert Syndrome: A Systematic Review and Meta-Analysis. [PDF]

Orthod Craniofac Res
ABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
Becerril Santos MC, Ongkosuwito EM, Papadopoulou AK, Antonarakis GS.   +3 more
europepmc   +2 more sources

The influence of closed sutures on cranial morphology in Apert and Crouzon syndromes: A quantitative analysis. [PDF]

J Anat
This quantitative study identified distinct cranial vault morphologies in Apert and Crouzon syndromes, with a larger anterior fossa in Apert and high variability in Crouzon, reflecting different patterns of suture closure. Abstract Craniosynostoses are congenital conditions characterized by premature suture fusions, altering skull growth and ...
Delassus O, Ben Bouazza L, Traoré AR, Uguen M, Boddaert N, Germanaud D, Mangin JF, Paternoster G, Taverne M, Khonsari RH.   +9 more
europepmc   +2 more sources

Computed tomography findings of Crouzon syndrome: A case report

Radiology Case Reports, 2022
Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ...
Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, Nury Tatiana Rincón Cuenca, MD, Angélica M. Sanabria Cano, MD, Maryi Fernanda Bermudez Sarmiento, MD, María F. Castro, MD, Andrés Felipe Herrera Ortiz, MD   +6 more
doaj   +1 more source

Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome [PDF]

, 2014
Background: Mutations of fibroblast growth factor receptor 2 (FGFR2) account for a higher proportion of genetic cases of craniosynostosis than any other gene, and are associated with a wide spectrum of severity of clinical problems.
Fenwick, A.L. (Aimée), Goos, J.A.C. (Jacqueline), Hoogeboom, A.J.M. (Jeannette), Lester, K.J. (Kathryn), Lord, H. (Helen), Mathijssen, I.M.J. (Irene), Ouweland, A.M.W. (Ans) van den, Rankin, J. (Julia), Wall, S.A. (Steven), Wilkie, A.O.M. (Andrew)   +9 more
core   +5 more sources

Three-Dimensional Evaluation of Dental Arches in Individuals with Syndromic Craniosynostosis

International Journal of Dentistry, 2023
Objective. Individuals with syndromic craniosynostosis present alterations in the dental arches due to anomalies caused by the early fusion of the craniomaxillary sutures.
Rayane de Oliveira Pinto, Cristiano Tonello, Adriano Porto Peixoto, Adriana Souza de Jesus, Ary dos Santos-Pinto, Dirceu Barnabé Raveli   +5 more
doaj   +1 more source

Mechanical properties of calvarial bones in a mouse model for craniosynostosis [PDF]

, 2015
The mammalian cranial vault largely consists of five flat bones that are joined together along their edges by soft fibrous tissues called sutures. Premature closure of the cranial sutures, craniosynostosis, can lead to serious clinical pathology unless ...
Babbs, Christian, Fagan, Michael J., Moazen, Mehran, Pauws, Erwin, Peskett, Emma   +4 more
core   +7 more sources

Crouzon syndrome: A comprehensive review and case report

Journal of Dr. NTR University of Health Sciences, 2017
Crouzon syndrome is an autosomal dominant disorder characterized by craniosynostosis of coronal and sagittal sutures. Crouzon syndrome is caused by mutation in the fibroblast growth factor receptor-2 (FGFR-2) gene.
Aditi Gaur, Sandhya Maheshwari, Sanjeev Kumar Verma, Mohammad Tariq   +3 more
doaj   +1 more source

Crouzon’s syndrome with adenotonsillitis: conventional surgery in altered anatomy. [PDF]

, 2013
Background/Objectives: Crouzon’s syndrome is characterized by premature closure of the cranial sutures, midface hypoplasia, orbital deformities & other associated abnormalities.Children with Crouzon syndrome frequently have obstructive sleep apnea ...
Appaji, Mohan, Devi, Pinky, MK, Goutham, Naik, Sarika s, Naik, Sudhir M, S, Ravishankar, SM, Annapurna   +6 more
core   +2 more sources

Imaging diagnosis of Crouzon syndrome in two cases confirmed on genetic studies - with a brief review

Indian Journal of Radiology and Imaging, 2019
Crouzon syndrome is the most common form of craniofacial dysostosis, characterised by a classical triad of abnormal skull shape, abnormal facies, and exophthalmos. The clinically overt dental abnormalities in these patients, distracts clinicians from the
Shabnam Bhandari Grover, Aanchal Bhayana, Hemal Grover, Seema Kapoor, Harish Chellani   +4 more
doaj   +1 more source

Midface advancement in an adult patient with Crouzon syndrome: Modified LeFort III + LeFort I osteotomy accompanied by genioplasty and nasal dorsum augmentation

Dental Research Journal, 2022
Crouzon syndrome is an autosomal dominant trait, leading to midface deficiency, undeveloped orbits, short nasal dorsum, and exophthalmos as the typical clinical features.
Milad Etemadi Sh, Golnaz Tajmiri
doaj   +1 more source