TY - JOUR
T1 - Heterozygous Variants in FREM2 Are Associated with Mesiodens, Supernumerary Teeth, Oral Exostoses, and Odontomas
AU - Kantaputra, Piranit Nik
AU - Tripuwabhrut, Kanich
AU - Anthonappa, Robert P.
AU - Chintakanon, Kanoknart
AU - Ngamphiw, Chumpol
AU - Adisornkanj, Ploy
AU - Porntrakulseree, Nop
AU - Olsen, Bjorn
AU - Intachai, Worrachet
AU - Hennekam, Raoul C.
AU - Vieira, Alexandre R.
AU - Tongsima, Sissades
N1 - Funding Information: This work was supported by Genomics Thailand Research Grant of Health Systems Research Institute. Publisher Copyright: © 2023 by the authors.
PY - 2023/4/1
Y1 - 2023/4/1
N2 - Background: Supernumerary teeth refer to extra teeth that exceed the usual number of dentitions. A mesiodens is a particular form of supernumerary tooth, which is located in the premaxilla region. The objective of the study was to investigate the genetic etiology of extra tooth phenotypes, including mesiodens and isolated supernumerary teeth. Methods: Oral and radiographic examinations and whole-exome sequencing were performed on every patient in our cohort of 122 patients, including 27 patients with isolated supernumerary teeth and 94 patients with mesiodens. A patient who had multiple supernumerary teeth also had odontomas. Results: We identified a novel (c.8498A>G; p.Asn2833Ser) and six recurrent (c.1603C>T; p.Arg535Cys, c.5852G>A; p.Arg1951His, c.6949A>T; p.Thr2317Ser; c.1549G>A; p.Val517Met, c.1921A>G; p.Thr641Ala, and c.850G>C; p.Val284Leu) heterozygous missense variants in FREM2 in eight patients with extra tooth phenotypes. Conclusions: Biallelic variants in FREM2 are implicated in autosomal recessive Fraser syndrome with or without dental anomalies. Here, we report for the first time that heterozygous carriers of FREM2 variants have phenotypes including oral exostoses, mesiodens, and isolated supernumerary teeth.
AB - Background: Supernumerary teeth refer to extra teeth that exceed the usual number of dentitions. A mesiodens is a particular form of supernumerary tooth, which is located in the premaxilla region. The objective of the study was to investigate the genetic etiology of extra tooth phenotypes, including mesiodens and isolated supernumerary teeth. Methods: Oral and radiographic examinations and whole-exome sequencing were performed on every patient in our cohort of 122 patients, including 27 patients with isolated supernumerary teeth and 94 patients with mesiodens. A patient who had multiple supernumerary teeth also had odontomas. Results: We identified a novel (c.8498A>G; p.Asn2833Ser) and six recurrent (c.1603C>T; p.Arg535Cys, c.5852G>A; p.Arg1951His, c.6949A>T; p.Thr2317Ser; c.1549G>A; p.Val517Met, c.1921A>G; p.Thr641Ala, and c.850G>C; p.Val284Leu) heterozygous missense variants in FREM2 in eight patients with extra tooth phenotypes. Conclusions: Biallelic variants in FREM2 are implicated in autosomal recessive Fraser syndrome with or without dental anomalies. Here, we report for the first time that heterozygous carriers of FREM2 variants have phenotypes including oral exostoses, mesiodens, and isolated supernumerary teeth.
KW - Fraser syndrome
KW - dental anomalies
KW - extra teeth
KW - mesiodens
KW - mesiodentes
KW - supernumerary tooth
KW - tooth formation
UR - http://www.scopus.com/inward/record.url?scp=85152700124&partnerID=8YFLogxK
U2 - https://doi.org/10.3390/diagnostics13071214
DO - https://doi.org/10.3390/diagnostics13071214
M3 - Article
C2 - 37046432
SN - 2075-4418
VL - 13
JO - Diagnostics
JF - Diagnostics
IS - 7
M1 - 1214
ER -