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病例报告:巨颌下颌第二前磨牙,一种遗传性牙齿异常。

Case report: Macrodont mandibular second premolars, a hereditary dental anomaly.

作者信息

Kyriazidou A, Haider D, Mason C, Parekh S, Bloch-Zupan A

机构信息

Eastman Dental Institute, University College of London, 256 Gray's Inn Road, London, WC1X 8LD, UK,

出版信息

Eur Arch Paediatr Dent. 2013 Dec;14(6):411-6. doi: 10.1007/s40368-013-0043-6. Epub 2013 Jun 5.

DOI:10.1007/s40368-013-0043-6
PMID:23737008
Abstract

BACKGROUND

Macrodontia or megadontia is a rare dental anomaly that refers to teeth that appear larger than normal. Generalised macrodontia may be associated with certain medical conditions and syndromes. Isolated macrodontia involves single teeth, might be the result of teeth fusion and is mainly seen in the incisor area.

CASE REPORTS

This paper describes two unrelated cases presenting with bilateral macrodont second lower premolars and the treatment provided. One case demonstrated the anomaly in both the patient and his father.

CONCLUSION

This case report suggests for the first time in the literature the genetic aetiology and heritability, as a possible autosomal dominant trait, of this rare dental anomaly.

摘要

背景

巨牙症是一种罕见的牙齿异常,指牙齿看起来比正常的大。全身性巨牙症可能与某些医学病症和综合征有关。孤立性巨牙症累及单个牙齿,可能是牙齿融合的结果,主要见于切牙区。

病例报告

本文描述了两例双侧下颌第二前磨牙巨牙症的无关病例及所提供的治疗。其中一例在患者及其父亲身上均表现出该异常。

结论

本病例报告首次在文献中提示了这种罕见牙齿异常的遗传病因及遗传性,可能为常染色体显性性状。

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1
Case report: Macrodont mandibular second premolars, a hereditary dental anomaly.病例报告:巨颌下颌第二前磨牙,一种遗传性牙齿异常。
Eur Arch Paediatr Dent. 2013 Dec;14(6):411-6. doi: 10.1007/s40368-013-0043-6. Epub 2013 Jun 5.
2
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引用本文的文献

1
Opportune management of a patient with a macrodont and supernumerary tooth.及时处理一位患有巨牙和多生牙的患者。
Aust Dent J. 2022 Sep;67(3):286-295. doi: 10.1111/adj.12903. Epub 2022 Mar 4.

本文引用的文献

1
Isolated bilateral macrodontia of mandibular second premolars: A case report.下颌第二前磨牙孤立性双侧巨牙症:一例报告。
Eur J Dent. 2012 Jul;6(3):330-4.
2
Nonsyndromic multiple hyperdontia in a series of 13 patients: epidemiologic and clinical considerations.13 例非综合征性多生牙患者的临床特征及流行病学分析
J Am Dent Assoc. 2012 Jun;143(6):e16-24. doi: 10.14219/jada.archive.2012.0243.
3
Odontometric evaluation of mandibular premolars with tooth shape deviation: a case-control study.下颌前磨牙牙冠形态偏斜的牙测量学评估:病例对照研究。
Angle Orthod. 2012 Sep;82(5):785-91. doi: 10.2319/110411-684.1. Epub 2012 Mar 7.
4
Congenital hemifacial hyperplasia.先天性半侧面部增生症
Contemp Clin Dent. 2011 Jul;2(3):261-4. doi: 10.4103/0976-237X.86492.
5
Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia.ANKRD11 基因突变会导致 KBG 综合征,其特征为智力障碍、骨骼畸形和巨牙症。
Am J Hum Genet. 2011 Aug 12;89(2):289-94. doi: 10.1016/j.ajhg.2011.06.007. Epub 2011 Jul 21.
6
Congenital infiltrating lipomatosis of the face: report of three cases and review of the literature.先天性面部浸润性脂肪瘤病:三例报告并文献复习。
J Craniomaxillofac Surg. 2010 Dec;38(8):610-4. doi: 10.1016/j.jcms.2010.02.014. Epub 2010 Mar 24.
7
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.单核苷酸多态性基因组扫描将耳齿综合征定位于11号染色体长臂13区,该位点的微缺失表明成纤维细胞生长因子3与牙齿和内耳疾病有关,而FADD与眼裂有关。
Hum Mol Genet. 2007 Oct 15;16(20):2482-93. doi: 10.1093/hmg/ddm204. Epub 2007 Jul 25.
8
The Ekman-Westborg and Julin trait: report of a case.埃克曼-韦斯特伯格和尤林特征:一例报告。
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Nov;102(5):659-62. doi: 10.1016/j.tripleo.2005.09.007. Epub 2006 Mar 24.
9
Extreme variations in the shape of mandibular premolars.
Am J Orthod Dentofacial Orthop. 2006 Sep;130(3):317-23. doi: 10.1016/j.ajodo.2005.01.022.
10
Otodental syndrome.耳牙综合征
Orphanet J Rare Dis. 2006 Mar 21;1:5. doi: 10.1186/1750-1172-1-5.