[14] |
Vieira TI, Cavalcanti YW, de Sousa SA,et al. Tooth wear prevalence in individuals with Down syndrome:A systematic review[J]. Clin Oral Investig, 2023, 27(3):943-953. DOI: 10.1007/s00784-022-04856-5.
|
[15] |
Cuoghi OA, Topolski F, Perciliano de Faria L,et al. Prevalence of dental anomalies in permanent dentition of brazilian individuals with down syndrome[J]. Open Dent J, 2016, 10:469-473. DOI: 10.2174/1874210601610010469.
|
[16] |
Aubert-Mucca M, Huber C, Baujat G,et al. Ellis-van creveld syndrome:Clinical and molecular analysis of 50 individuals[J]. J Med Genet, 2022:jmg-2022-108435. DOI: 10.1136/jmg-2022-108435.
|
[17] |
Shaik S, Raviraj J, Dirasantchu S,et al. Ellis-van Creveld syndrome with unusual oral and dental findings:A rare clinical entity[J]. Dent Res J(Isfahan), 2016, 13(2):193-197. DOI: 10.4103/1735-3327.178213.
|
[18] |
Elmubarak NA. Genetic risk of talon cusp:Talon cusp in five siblings[J]. Case Rep Dent, 2019:3080769. DOI: 10.1155/2019/3080769.
|
[19] |
Panigrahi A, Panigrahi RG, Srilatha KT,et al. Non syndromic familial bilateral decidious taurodontism:A first case report[J]. J Clin Diagn Res, 2014, 8(12):ZD01-ZD02. DOI: 10.7860/JCDR/2014/8527.5228.
|
[20] |
Poswar FO, Henriques Nehm J, Kubaski F,et al. Diagnosis and emerging treatment strategies for mucopolysaccharidosis Ⅶ(Sly Syndrome)[J]. Ther Clin Risk Manag, 2022, 18:1143-1155. DOI: 10.2147/TCRM.S351300.
|
[21] |
Kantaputra PN, Smith LJ, Casal ML,et al. Oral manifestations in patients and dogs with mucopolysaccharidosis Type Ⅶ[J]. Am J Med Genet A, 2019, 179(3):486-493. DOI: 10.1002/ajmg.a.61034.
|
[22] |
Krishnamoorthy S, Gopikrishna V. Endodontic management of a hypertaurodontic tooth associated with 48,XXYY syndrome:A review and case report[J]. J Conserv Dent, 2015, 18(3):265-268. DOI: 10.4103/0972-0707.157269.
|
[23] |
Belling K, Russo F, Jensen AB,et al. Klinefelter syndrome comorbidities linked to increased X chromosome gene dosage and altered protein interactome activity[J]. Hum Mol Genet, 2017, 26(7):1219-1229. DOI: 10.1093/hmg/ddx014.
|
[24] |
Jaspers MT,Witkop CJ Jr. Taurodontism,an isolated trait associated with syndromes and X-chromosomal aneuploidy[J]. Am J Hum Genet,1980,32(3):396-413.
|
[25] |
Passarelli PC, Pasquantonio G, Manicone PF,et al. Orofacial signs and dental abnormalities in patients with Mulvihill-Smith syndrome:A literature review on this rare progeroid pathology [J]. Medicine(Baltimore), 2018, 97(18):e0656. DOI: 10.1097/MD.0000000000010656.
|
[26] |
Sobti G, Chaudhry A, Thanvi J,et al. Co-occurrence of taurodontism in nonsyndromic cleft lip and palate patients in subset of indian population:A case-control study using CBCT [J]. Cleft Palate Craniofac J, 2022:10556656221089159. DOI: 10.1177/10556656221089159.
|
[27] |
Awadh W, Pegelow M, Heliovaara A,et al. Taurodontism in the first permanent molars in Van der Woude syndrome compared to isolated cleft palate[J]. Eur J Orthod, 2021, 43(1):29-35. DOI: 10.1093/ejo/cjaa014.
|
[28] |
Fonseca-Souza G, de Oliveira LB, Wambier LM,et al. Tooth abnormalities associated with non-syndromic cleft lip and palate:Systematic review and meta-analysis[J]. Clin Oral Investig, 2022, 26(8):5089-5103. DOI: 10.1007/s00784-022-04540-8.
|
[29] |
|
[30] |
Fons Romero JM, Star H, Lav R,et al. The impact of the eda pathway on tooth root development[J]. J Dent Res, 2017, 96(11):1290-1297. DOI: 10.1177/0022034517725692.
|
[31] |
Sohn WJ, Choi MA, Yamamoto H,et al. Contribution of mesenchymal proliferation in tooth root morphogenesis[J]. J Dent Res, 2014, 93(1):78-83. DOI: 10.1177/0022034513511247.
|
[32] |
|
[33] |
Kim TH, Bae CH, Yang S,et al. Nfic regulates tooth root patterning and growth[J]. Anat Cell Biol, 2015, 48(3):188-194. DOI: 10.5115/acb.2015.48.3.188.
|
[34] |
Bergendal B, Norderyd J, Zhou X,et al. Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency[J]. BMC Med Genet, 2016, 17(1):88. DOI: 10.1186/s12881-016-0349-4.
|
[35] |
Yang J, Wang SK, Choi M,et al. Taurodontism,variations in tooth number,and misshapened crowns in Wnt10a null mice and human kindreds[J]. Mol Genet Genomic Med, 2015, 3(1):40-58. DOI: 10.1002/mgg3.111.
|
[36] |
Yu M, Liu Y, Wang Y,et al. Epithelial Wnt10a is essential for tooth root furcation morphogenesis[J]. J Dent Res, 2020, 99(3):311-319. DOI: 10.1177/0022034519897607.
|
[37] |
Kantaputra P, Jatooratthawichot P, Kottege N,et al. DKK1 is a strong candidate for mesiodens and taurodontism[J]. Clin Genet, 2023. DOI: 10.1111/cge.14295.
|
[38] |
Sheng L, Hao SL, Yang WX,et al. The multiple functions of kinesin-4 family motor protein KIF4 and its clinical potential[J]. Gene, 2018, 678:90-99. DOI: 10.1016/j.gene.2018.08.005.
|
[39] |
Gowans LJJ, Cameron-Christie S, Slayton RL,et al. Missense Pathogenic variants in KIF4A affect dental morphogenesis resulting in X-linked taurodontism,microdontia and dens-invaginatus[J]. Front Genet, 2019, 10:800. DOI: 10.3389/fgene.2019.00800.
|
[40] |
Zheng J, Liu H, Zhan Y,et al. Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders[J]. Mol Genet Genomic Med, 2019, 7(6):e704. DOI: 10.1002/mgg3.704.
|
[41] |
Wang J, Feng JQ. Signaling pathways critical for tooth root formation[J]. J Dent Res, 2017, 96(11):1221-1228. DOI: 10.1177/0022034517717478.
|
[42] |
Borges AH,Mamede-Neto I,Volpato LE,et al. Using cone beam computed tomography images to diagnose multiple taurodontisms [J]. Gen Dent,2014,62(2):e20-e22.
|
[43] |
|
[44] |
|
[45] |
Aydin H, Mobaraki S. Comparison of root and canal anatomy of taurodont and normal molar teeth:A retrospective cone-beam computed tomography study[J]. Arch Oral Biol, 2021, 130:105242. DOI: 10.1016/j.archoralbio.2021.105242.
|
[1] |
Ahmed HMA, Dummer PMH. A new system for classifying tooth,root and canal anomalies[J]. Int Endod J, 2018, 51(4):389-404. DOI: 10.1111/iej.12867.
|
[2] |
Feichtinger C, Rossiwall B. Taurodontism in human sex chromosome aneuploidy[J]. Arch Oral Biol, 1977, 22(5):327-329. DOI: 10.1016/0003-9969(77)90031-0.
|
[3] |
|
[4] |
Shaw JC. Taurodont teeth in South African races[J]. J Anat,1928,62(Pt 4):476-498.1.
|
[5] |
Keene HJ. A morphologic and biometric study of taurodontism in a contemporary population[J]. Am J Phys Anthropol,1966,25:208-209.
|
[6] |
Shifman A, Chanannel I. Prevalence of taurodontism found in radiographic dental examination of 1,200 young adult Israeli patients[J]. Community Dent Oral Epidemiol, 1978, 6(4):200-203. DOI: 10.1111/j.1600-0528.1978.tb01150.x.
|
[7] |
Jafarzadeh H, Azarpazhooh A, Mayhall JT. Taurodontism:A review of the condition and endodontic treatment challenges[J]. Int Endod J, 2008, 41(5):375-388. DOI: 10.1111/j.1365-2591.2008.01388.x.
|
[8] |
Shipley GP, Kindscher K. Evidence for the paleoethnobotany of the neanderthal:A review of the literature[J]. Scientifica (Cairo), 2016:8927654. DOI: 10.1155/2016/8927654.
|
[9] |
Benazzi S, Nguyen HN, Kullmer O,et al. Exploring the biomechanics of taurodontism[J]. J Anat, 2015, 226(2):180-188. DOI: 10.1111/joa.12260.
|
[10] |
Lucas-Sánchez M, Serradell JM, Comas D. Population history of North Africa based on modern and ancient genomes[J]. Hum Mol Genet, 2021, 30(R1):R17-R23. DOI: 10.1093/hmg/ddaa261.
|
[11] |
Hublin JJ, Roebroeks W. Ebb and flow or regional extinctions?On the character of Neandertal occupation of northern environments [J]. Comptes Rendus Palevol, 2009, 8(5):503-509. DOI: 10.1016/j.crpv.2009.04.001.
|
[12] |
Whitehouse LLE, Smith CEL, Poulter JA,et al. Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome[J]. Oral Dis, 2019, 25(1):182-191. DOI: 10.1111/odi.12955.
|
[13] |
Jagtap R, Alansari R, Ruprecht A,et al. Trichodentoosseous syndrome:A case report and review of literature[J]. BJR Case Rep, 2019, 5(4):20190039. DOI: 10.1259/bjrcr.20190039.
|
[46] |
Pach J, Regulski PA, Tomczyk J,et al. Clinical implications of a diagnosis of taurodontism:A literature review[J]. Adv Clin Exp Med, 2022, 31(12):1385-1389. DOI: 10.17219/acem/152120.
|