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Characteristic dental pattern with hypodontia and short roots in Fraser Syndrome

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dc.contributor.author Kunz, F.
dc.contributor.author Kayserili, H.
dc.contributor.author Midro, A.
dc.contributor.author de Silva, D.
dc.contributor.author Basnayake, S.
dc.contributor.author Güven, Y.
dc.contributor.author Borys, J.
dc.contributor.author Schanze, D.
dc.contributor.author Stellzig-Eisenhauer, A.
dc.contributor.author Bloch-Zupan, A.
dc.contributor.author Zenker, M.
dc.date.accessioned 2020-07-10T04:13:30Z
dc.date.available 2020-07-10T04:13:30Z
dc.date.issued 2020
dc.identifier.citation American Journal of Medical Genetics. 2020;182(7):1681-1689. [Epub 2020 June] en_US
dc.identifier.issn 1552-4825 (Print)
dc.identifier.issn 1552-4833 (Electronic)
dc.identifier.issn 1552-4825 (Linking)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/21136
dc.description Indexed in MEDLINE en_US
dc.description.abstract ABSTRACT: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 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. KEYWORDS: Fraser syndrome; dental roots; hypodontia; orodental health; taurodontism. en_US
dc.language.iso en_US en_US
dc.publisher Wiley-Liss en_US
dc.subject Dental Pattern en_US
dc.title Characteristic dental pattern with hypodontia and short roots in Fraser Syndrome en_US
dc.type Article en_US


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