دورية أكاديمية
أعرض في EDS

Evaluation of dental maturity in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.

التفاصيل البيبلوغرافية
العنوان: Evaluation of dental maturity in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.
المؤلفون: Choi TM; Department of Oral Maxillofacial Surgery, Special Dental Care and Orthodontics, Dutch Craniofacial Center, Erasmus MC, University Medical Center Rotterdam, The Netherlands., Kramer GJC; Department of Orthodontics, Academic Center for Dentistry Amsterdam, University of Amsterdam and Vrije Universiteit Amsterdam, The Netherlands., Goos JAC; Department of Plastic and Reconstructive Surgery and Hand Surgery, Dutch Craniofacial Center, Erasmus MC, University Medical Center Rotterdam, The Netherlands., Mathijssen IMJ; Department of Plastic and Reconstructive Surgery and Hand Surgery, Dutch Craniofacial Center, Erasmus MC, University Medical Center Rotterdam, The Netherlands., Wolvius EB; Department of Oral Maxillofacial Surgery, Special Dental Care and Orthodontics, Dutch Craniofacial Center, Erasmus MC, University Medical Center Rotterdam, The Netherlands., Ongkosuwito EM; Department of Oral Maxillofacial Surgery, Special Dental Care and Orthodontics, Dutch Craniofacial Center, Erasmus MC, University Medical Center Rotterdam, The Netherlands.
المصدر: European journal of orthodontics [Eur J Orthod] 2022 May 24; Vol. 44 (3), pp. 287-293.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 7909010 Publication Model: Print Cited Medium: Internet ISSN: 1460-2210 (Electronic) Linking ISSN: 01415387 NLM ISO Abbreviation: Eur J Orthod Subsets: MEDLINE
أسماء مطبوعة: Publication: Oxford : Oxford University Press
Original Publication: [London] Churchill Livingstone.
مواضيع طبية MeSH: Acrocephalosyndactylia*/diagnostic imaging , Acrocephalosyndactylia*/surgery , Craniosynostoses*/complications , Craniosynostoses*/diagnostic imaging , Craniosynostoses*/surgery, Basic Helix-Loop-Helix Transcription Factors ; Child ; Child, Preschool ; Humans ; Netherlands ; Syndrome
مستخلص: Objectives: To determine whether dental maturity (dental development) was delayed in patients with Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis, compared with a Dutch control group without syndromes.
Materials and Methods: This study included 60 patients (38 patients with Muenke syndrome, 17 patients with Saethre-Chotzen syndrome, and 5 with TCF12-related craniosynostosis), aged 5.8-16.8 years that were treated at the Department of Oral Maxillofacial Surgery, Special Dental Care, and Orthodontics, in Sophia Children's Hospital, Erasmus University Medical Center, Rotterdam, the Netherlands. Dental age was calculated according to Demirjian's index of dental maturity. The control group included 451 children without a syndrome.
Results: Compared with the control group, dental development was delayed by an average of one year in 5- to 8-year-old patients with Muenke syndrome (P = 0.007) and in 8- to 10-year-old patients with Saethre-Chotzen syndrome (P = 0.044), but not in patients with TCF12-related craniosynostosis.
Conclusions: Our results indicated that dental development was delayed by one year, on average, in patients with Muenke syndrome and Saethre-Chotzen syndrome, compared with a Dutch control group without syndromes.
Implications: Our findings have improved the understanding of dental development in patients with Muenke and Saethre-Chotzen syndrome. These results can provide guidance on whether the orthodontist needs to consider growth disturbances related to dental development.
(© The Author(s) 2021. Published by Oxford University Press on behalf of the European Orthodontic Society.)
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المشرفين على المادة: 0 (Basic Helix-Loop-Helix Transcription Factors)
142661-93-6 (TCF12 protein, human)
SCR Disease Name: Muenke Syndrome
تواريخ الأحداث: Date Created: 20210823 Date Completed: 20220525 Latest Revision: 20230916
رمز التحديث: 20230916
مُعرف محوري في PubMed: PMC9127722
DOI: 10.1093/ejo/cjab056
PMID: 34424951
قاعدة البيانات: MEDLINE
الوصف
تدمد:1460-2210
DOI:10.1093/ejo/cjab056