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South European journal of orthodontics and dentofacial research, Vol. 3 No. 1, 2016.

Pregledni rad
https://doi.org/10.5937/sejodr3-15220

The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports

Lazić, E.
Jakovljević, A.
Nikodijević Latinović, A.
Nedeljković, N.

Puni tekst: engleski, pdf (598 KB) str. 24-33 preuzimanja: 272* citiraj
APA 6th Edition
Lazić, E., Jakovljević, A., Nikodijević Latinović, A. i Nedeljković, N. (2016). The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports. South European journal of orthodontics and dentofacial research, 3 (1), 24-33. https://doi.org/10.5937/sejodr3-15220
MLA 8th Edition
Lazić, E., et al. "The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports." South European journal of orthodontics and dentofacial research, vol. 3, br. 1, 2016, str. 24-33. https://doi.org/10.5937/sejodr3-15220. Citirano 16.02.2019.
Chicago 17th Edition
Lazić, E., Jakovljević, A., Nikodijević Latinović, A. i Nedeljković, N.. "The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports." South European journal of orthodontics and dentofacial research 3, br. 1 (2016): 24-33. https://doi.org/10.5937/sejodr3-15220
Harvard
Lazić, E., et al. (2016). 'The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports', South European journal of orthodontics and dentofacial research, 3(1), str. 24-33. doi: https://doi.org/10.5937/sejodr3-15220
Vancouver
Lazić, E., Jakovljević, A., Nikodijević Latinović, A., Nedeljković, N.. The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports. South European journal of orthodontics and dentofacial research [Internet]. 2016 [pristupljeno 16.02.2019.];3(1):24-33. doi: https://doi.org/10.5937/sejodr3-15220
IEEE
Lazić, E., Jakovljević, A., Nikodijević Latinović, A. i Nedeljković, N., "The characteristics of craniofacial and cervicovertebral morphology in different genetic syndromes – a literature review and three case reports", South European journal of orthodontics and dentofacial research, vol.3, br. 1, str. 24-33, 2016. [Online]. doi: https://doi.org/10.5937/sejodr3-15220

Sažetak
Introduction: Patients with genetic syndromes were characterized by variety of skeletal craniofacial and cervicovertebral morphology. Skeletal anomalies are recognized concomitants of the various genetic syndromes. The aim of the study was to review the current literature on this topic and to present the characteristics of craniofacial and cervicovertebral morphology and subsequent anomalies in three patients with Crouzon syndrome, Treacher Collins syndrome and cleidocranial dysplasia.
Materials and Methods: A comprehensive electronic search was performed using PubMed via Medline, Web of Science and SCOPUS.A manual search involved references form articles retrieved for possible inclusion. There were no restrictions as to date of publication, study design or language. The search, evaluation of relevant articles, and their critical appraisal were performed by two independent judges. Discrepancies between reviewers were resolved through a consensus with a third party. Case reports: Additionally, this paper presents a radiographic analysis of craniofacial and cervicovertebral morphology in patients with cleidocranial dysplasia, Crouzon, and Treacher Collins syndromes. The most characteristic findings of cervicovertebral morphology were the presence of cervical spine fusions in all three patients. The intervertebral fusions in patients with Crouzon and TreacherCollins syndromes have been characterized with "block vertebrae". Cervicovertebral complex of the patient with cleidocranialdysplasia is characterized by delayed mineralization of vertebral bodies (C1–C7).
Results: Although craniofacial and cervicovertebral anomalies in presented syndromes have different phenotype expression, the vast majority of cases are caused by mutations in specific, syndrome-related genes (FGFR2, FGFR3, RUNX2, TCOF1, POLR1C,POLR1D). Craniofacial anomalies, that include changes in development of hard and soft tissues, were considered as traditional concomitant of presented syndromes. Apart from these changes, cervicovertebral region could also be affected. Recent reports show different changes in vertebral structure (delayed mineralization) and unphysiological relations (cervical spine fusions).
Conclusion: The limitation of cervical range of motion resulting from these anomalies may have clinical significance on multidisciplinary management approach in these patients. Recent progress in dentistry resulted in better diagnostic and therapeutic options and outcomes for individuals with genetic syndromes.

Hrčak ID: 156764

URI
https://hrcak.srce.hr/156764

Posjeta: 400 *