Characteristic dental pattern with hypodontia and short roots in Fraser syndrome

Please always quote using this URN: urn:nbn:de:bvb:20-opus-216147
  • Fraser syndrome (FS) is a rare autosomal recessive multiple congenital malformation syndrome characterized by cryptophthalmos, cutaneous syndactyly, renal agenesis, ambiguous genitalia, and laryngotracheal anomalies. It is caused by biallelic mutations of FRAS1, FREM2, and GRIP1 genes, encoding components of a protein complex that mediates embryonic epithelial–mesenchymal interactions. Anecdotal reports have described abnormal orodental findings in FS, but no study has as yet addressed the orodental findings of FS systematically. We reviewedFraser syndrome (FS) is a rare autosomal recessive multiple congenital malformation syndrome characterized by cryptophthalmos, cutaneous syndactyly, renal agenesis, ambiguous genitalia, and laryngotracheal anomalies. It is caused by biallelic mutations of FRAS1, FREM2, and GRIP1 genes, encoding components of a protein complex that mediates embryonic epithelial–mesenchymal interactions. Anecdotal reports have described abnormal orodental findings in FS, but no study has as yet addressed the orodental findings of FS systematically. We reviewed dental radiographs of 10 unrelated patients with FS of different genetic etiologies. Dental anomalies were present in all patients with FS and included hypodontia, dental crowding, medial diastema, and retained teeth. A very consistent pattern of shortened dental roots of most permanent teeth as well as altered length/width ratio with shortened dental crowns of upper incisors was also identified. These findings suggest that the FRAS1–FREM complex mediates critical mesenchymal–epithelial interactions during dental crown and root development. The orodental findings of FS reported herein represent a previously underestimated manifestation of the disorder with significant impact on orodental health for affected individuals. Integration of dentists and orthodontists into the multidisciplinary team for management of FS is therefore recommended.show moreshow less

Download full text files

Export metadata

Additional Services

Share in Twitter Search Google Scholar Statistics
Metadaten
Author: Felix Kunz, Hülya Kayserili, Alina Midro, Deepthi de Silva, Sriyani Basnayake, Yeliz Güven, Jan Borys, Denny Schanze, Angelika Stellzig‐Eisenhauer, Agnes Bloch‐Zupan, Martin Zenker
URN:urn:nbn:de:bvb:20-opus-216147
Document Type:Journal article
Faculties:Medizinische Fakultät / Poliklinik für Zahnärztliche Prothetik
Language:English
Parent Title (English):American Journal of Medical Genetics Part A
Year of Completion:2020
Volume:182
Issue:7
First Page:1681
Last Page:1689
Source:American Journal of Medical Genetics Part A 2020, 182(7):1681–1689. DOI: 10.1002/ajmg.a.61610
DOI:https://doi.org/10.1002/ajmg.a.61610
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Tag:Fraser syndrome; dental roots; hypodontia; orodental health; taurodontism
Release Date:2021/07/02
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International