West China Journal of Stomatology ›› 2022, Vol. 40 ›› Issue (4): 483-488.doi: 10.7518/hxkq.2022.04.017
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Received:
2021-06-29
Revised:
2022-04-15
Online:
2022-07-25
Published:
2022-07-27
Contact:
Li Yuangao.
E-mail:chenxue851207@163.com;H12508@sina.com
CLC Number:
Chen Xue, Li Yuangao.. Non-syndromic familial congenital dental deficiency: two cases report[J]. West China Journal of Stomatology, 2022, 40(4): 483-488.
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1 | Schalk-van der Weide Y, Steen WH, Bosman F. Distribution of missing teeth and tooth morphology in patients with oligodontia[J]. ASDC J Dent Child, 1992, 59(2): 133-140. |
2 | Yin W, Bian Z. The gene network underlying hypodontia[J]. J Dent Res, 2015, 94(7): 878-885. |
3 | Thesleff I. The genetic basis of tooth development and dental defects[J]. Am J Med Genet A, 2006, 140(23):2530-2535. |
4 | Militi D, Militi A, Cutrupi MC, et al. Genetic basis of non syndromic hypodontia: a DNA investigation performed on three couples of monozygotic twins about PAX9 mutation[J]. Eur J Paediatr Dent, 2011, 12(1): 21-24. |
5 | Arte S, Nieminen P, Apajalahti S, et al. Characteristics of incisor-premolar hypodontia in families[J]. J Dent Res, 2001, 80(5): 1445-1450. |
6 | Pirinen S, Kentala A, Nieminen P, et al. Recessively inherited lower incisor hypodontia[J]. J Med Genet, 2001, 38(8): 551-556. |
7 | Erpenstein H, Pfeiffer RA. Sex-linked-dominant hereditary reduction in number of teeth[J]. Humangenetik, 1967, 4(3): 280-293. |
8 | Shimizu T, Maeda T. Prevalence and genetic basis of tooth agenesis[J]. Jpn Dent Sci Rev, 2009, 45(1): 52-58. |
9 | Chung CJ, Han JH, Kim KH. The pattern and prevalence of hypodontia in Koreans[J]. Oral Dis, 2008, 14(7): 620-625. |
10 | Xin TY, Zhang T, Li Q, et al. A novel mutation of MSX1 in oligodontia inhibits odontogenesis of dental pulp stem cells via the ERK pathway[J]. Stem Cell Res Ther, 2018, 9(1): 221. |
11 | Nieminen P, Arte S, Tanner D, et al. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia[J]. Eur J Hum Genet, 2001, 9(10): 743-746. |
12 | Lidral AC, Reising BC. The role of MSX1 in human tooth agenesis[J]. J Dent Res, 2002, 81(4): 274-278. |
13 | Bonczek O, Balcar VJ, Šerý O. PAX9 gene mutations and tooth agenesis: a review[J]. Clin Genet, 2017, 92(5): 467-476. |
14 | Fauzi NH, Ardini YD, Zainuddin Z, et al. A review on non-syndromic tooth agenesis associated with PAX9 mutations[J]. Jpn Dent Sci Rev, 2018, 54(1): 30-36. |
15 | Wong SW, Han D, Zhang H, et al. Nine novel PAX9 mutations and a distinct tooth agenesis genotype-phenotype[J]. J Dent Res, 2018, 97(2): 155-162. |
16 | Cobourne MT. Familial human hypodontia: is it all in the genes[J]. Br Dent J, 2007, 203(4): 203-208. |
17 | Liu HC, Ding TT, Zhan Y, et al. A novel AXIN2 missense mutation is associated with non-syndromic oligodontia[J]. PLoS One, 2015, 10(9): e0138221. |
18 | Wong S, Liu HC, Bai BJ, et al. Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia[J]. Arch Oral Biol, 2014, 59(3): 349-353. |
19 | Marvin ML, Mazzoni SM, Herron CM, et al. AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome[J]. Am J Med Genet A, 2011, 155A(4): 898-902. |
20 | Rakhshan V. Congenitally missing teeth (hypodontia): a review of the literature concerning the etiology, prevalence, risk factors, patterns and treatment[J]. Dent Res J (Isfahan), 2015, 12(1): 1-13. |
21 | Goya HA, Tanaka S, Maeda T, et al. An orthopantomographic study of hypodontia in permanent teeth of Japanese pediatric patients[J]. J Oral Sci, 2008, 50(2): 143-150. |
22 | Hedayati Z, Dashlibrun YN. The prevalence and distribution pattern of hypodontia among orthodontic patients in Southern Iran[J]. Eur J Dent, 2013, 7(): S078-S082. |
23 | Vahid-Dastjerdi E, Borzabadi-Farahani A, Mahdian M, et al. Non-syndromic hypodontia in an Iranian orthodontic population[J]. J Oral Sci, 2010, 52(3): 455-461. |
24 | Behr M, Proff P, Leitzmann M, et al. Survey of congenitally missing teeth in orthodontic patients in Eastern Bavaria[J]. Eur J Orthod, 2011, 33(1): 32-36. |
25 | Sterzik G, Steinbicker V, Karl N. The etiology of hypodontia[J]. Fortschr Kieferorthop, 1994, 55(2): 61-69. |
26 | Polder BJ, Van’t Hof MA, van der Linden FP, et al. A Meta-analysis of the prevalence of dental agenesis of permanent teeth[J]. Community Dent Oral Epidemiol, 2004, 32(3): 217-226. |
27 | Sisman Y, Uysal T, Gelgor IE. Hypodontia. Does the prevalence and distribution pattern differ in orthodontic patients[J]. Eur J Dent, 2007, 1(3): 167-173. |
28 | Amini F, Rakhshan V, Babaei P. Prevalence and pattern of hypodontia in the permanent dentition of 3 374 Iranian orthodontic patients[J]. Dent Res J (Isfahan), 2012, 9(3): 245-250. |
29 | Tallón-Walton V, Nieminen P, Arte S, et al. An epidemiological study of dental agenesis in a primary health area in Spain: estimated prevalence and associated factors[J]. Med Oral Patol Oral Cir Bucal, 2010, 15(4): e569-e574. |
30 | Rakhshan V. Meta-analysis and systematic review of factors biasing the observed prevalence of congenitally missing teeth in permanent dentition excluding third molars[J]. Prog Orthod, 2013, 14: 33. |
31 | Sheikhi M, Sadeghi MA, Ghorbanizadeh S. Prevalence of congenitally missing permanent teeth in Iran[J]. Dent Res J (Isfahan), 2012, 9(): 105-111. |
32 | Endo T, Ozoe R, Kubota M, et al. A survey of hypodontia in Japanese orthodontic patients[J]. Am J Orthod Dentofacial Orthop, 2006, 129(1): 29-35. |
33 | Rahardjo P. Prevalence of hypodontia in Chinese orthodontic patients[J]. Dent J (Maj Ked Gigi), 2006, 39(4): 147-150. |
34 | Rakhshan V, Rakhshan H. Meta-analysis and systematic review of the number of non-syndromic congenitally missing permanent teeth per affected individual and its influencing factors[J]. Eur J Orthod, 2016, 38(2): 170-177. |
35 | Heuberer S, Ulm C, Zechner W, et al. Patterns of congenitally missing teeth of non-syndromic and syndromic patients treated at a single-center over the past thirty years[J]. Arch Oral Biol, 2019, 98: 140-147. |
36 | De Coster PJ, Marks LA, Martens LC, et al. Dental agenesis: genetic and clinical perspectives[J]. J Oral Pathol Med, 2009, 38(1): 1-17. |
37 | Wisth PJ, Thunold K, Böe OE. Frequency of hypodontia in relation to tooth size and dental arch width[J]. Acta Odontol Scand, 1974, 32(3): 201-206. |
38 | Kan WY, Seow WK, Holcombe T. Taurodontism in children with hypodontia and supernumerary teeth: a case control study[J]. Pediatr Dent, 2010, 32(2): 134-140. |
39 | Behr M, Driemel O, Mertins V, et al. Concepts for the treatment of adolescent patients with missing permanent teeth[J]. Oral Maxillofac Surg, 2008, 12(2): 49-60. |
40 | 冯海兰. 先天性缺牙的口腔修复治疗Ⅲ. 先天性缺牙的修复治疗原则[J]. 中华口腔医学杂志, 2011, 46(5): 306-310. |
Feng HL. Prosthodontic treatment of congenital missing teeth Ⅲ. Principles of prosthodontic treatment of congenital missing teeth[J]. Chin J Stomatol, 2011, 46(5): 306-310. | |
41 | DE Stefani A, Bruno G, Frezza A, et al. Association between teeth agenesis and Angle’s classes in an Italian population[J]. Minerva Dent Oral Sci, 2021, 70(1): 21-25. |
42 | Papandreas SG, Buschang PH, Alexander RG, et al. Physiologic drift of the mandibular dentition following first premolar extractions[J]. Angle Orthod, 1993, 63(2): 127-134. |
43 | Northway WM. The nuts and bolts of hemisection treatment: managing congenitally missing mandibular second premolars[J]. Am J Orthod Dentofacial Orthop, 2005, 127(5): 606-610. |
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[11] | . [J]. , 1994, 12(02): 0-. |
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