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恒牙列非综合征性少牙畸形:一例报告

Non-syndromic oligodontia in permanent dentition: a case report.

作者信息

Pannu P, Galhotra V, Ahluwalai P, Gambhir R S

机构信息

Gian Sagar Dental College and Hospital - Pediatric and Preventive Dentistry, Rajpura, India.

Sector 7C, Chandigarh, Chandigarh 160019, India.

出版信息

Ghana Med J. 2014 Sep;48(3):173-6. doi: 10.4314/gmj.v48i3.10.

DOI:10.4314/gmj.v48i3.10
PMID:25709129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4335449/
Abstract

Tooth agenesis is one of the most common congenital anomalies seen in humans. Although absence of one or more teeth is common but absence of multiple teeth is rare. Oligodontia is a rare developmental anomaly, involving agenesis of six or more permanent teeth, excluding the third molars. The reported prevalence of oligodontia in permanent dentition is 0.14%. Oligodontia can present as an isolated condition or as a part of a syndrome. The present case report highlights a unique case of non syndromic oligodontia, with agenesis of four permanent incisors, left permanent canine and right second premolar in the mandibular arch and its management with a novel fixed functional prosthetic appliance. Prosthetic rehabilitation is an urgent need for these kind of patients so that they do not suffer from masticatory and esthetic problems which can eventually lower the self esteem of individuals.

摘要

牙齿发育不全是人类最常见的先天性异常之一。虽然一颗或多颗牙齿缺失很常见,但多颗牙齿缺失却很罕见。少牙畸形是一种罕见的发育异常,涉及六颗或更多恒牙的发育不全,不包括第三磨牙。报道的恒牙列少牙畸形患病率为0.14%。少牙畸形可表现为孤立病症或作为综合征的一部分。本病例报告突出了一例非综合征性少牙畸形的独特病例,下颌牙弓中四颗恒切牙、左侧恒尖牙和右侧第二前磨牙发育不全,并采用新型固定功能性修复装置进行治疗。对于这类患者来说,修复性康复是迫切需要的,这样他们就不会遭受咀嚼和美观问题,而这些问题最终可能会降低个人的自尊心。

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引用本文的文献

1
Use of a Modified Nance Appliance for Esthetic Rehabilitation of a Child Patient with Rare Nonfamilial and Nonsyndromic Oligodontia.使用改良式南斯矫治器对一名患有罕见非家族性和非综合征性少牙畸形的儿童患者进行美学修复。
Case Rep Dent. 2021 Jul 21;2021:5444257. doi: 10.1155/2021/5444257. eCollection 2021.

本文引用的文献

1
Long-term follow-up of implant treatment for oligodontia in an actively growing individual: a clinical report.种植治疗个别先天缺牙患者的长期随访:一份临床报告。
J Prosthet Dent. 2012 Nov;108(5):279-85. doi: 10.1016/S0022-3913(12)60176-0.
2
Revision of "A 223-kb de novo deletion of PAX9 in a patient with oligodontia".《一名少牙畸形患者中PAX9基因223kb新发缺失的修正》
J Craniofac Surg. 2012 Mar;23(2):e149-51. doi: 10.1097/SCS.0b013e31824cdcdd.
3
Non-syndromic oligodontia with a novel mutation of PAX9.非综合征型缺牙症伴 PAX9 基因新突变。
J Dent Res. 2011 Mar;90(3):382-6. doi: 10.1177/0022034510390042. Epub 2010 Nov 22.
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Dental agenesis: genetic and clinical perspectives.牙发育不全:遗传学与临床视角
J Oral Pathol Med. 2009 Jan;38(1):1-17. doi: 10.1111/j.1600-0714.2008.00699.x. Epub 2008 Sep 1.
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Tooth agenesis: from molecular genetics to molecular dentistry.牙齿发育不全:从分子遗传学至分子牙科学
J Dent Res. 2008 Jul;87(7):617-23. doi: 10.1177/154405910808700715.
6
Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia.探究三名患有严重少牙症的姐妹中多颗牙齿缺失的病因。
Orthod Craniofac Res. 2008 Feb;11(1):24-31. doi: 10.1111/j.1601-6343.2008.00410.x.
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Congenitally missing mandibular incisors and mandibular symphysis morphology.先天性缺失下颌切牙与下颌联合形态
Angle Orthod. 2007 Nov;77(6):1079-84. doi: 10.2319/020106-37.1.
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Treatment of severe hypodontia-oligodontia--an interdisciplinary concept.严重牙列稀疏-少牙畸形的治疗——一个跨学科理念。
Int J Oral Maxillofac Surg. 2007 Jun;36(6):473-80. doi: 10.1016/j.ijom.2007.01.021. Epub 2007 Apr 12.
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Implants in children with ectodermal dysplasia: a case report and literature review.外胚层发育不良患儿的植入物:病例报告及文献综述
Clin Oral Implants Res. 2007 Feb;18(1):140-6. doi: 10.1111/j.1600-0501.2006.01180.x.
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Treatment outcomes for adolescent ectodermal dysplasia patients treated with dental implants.牙种植体治疗青少年外胚层发育不良患者的治疗效果。
Int J Paediatr Dent. 2005 Jul;15(4):241-8. doi: 10.1111/j.1365-263X.2005.00610.x.