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磨牙-切牙-恒前牙畸形:病例报告和病例系列的系统综述。

Molar-root incisor malformation - a systematic review of case reports and case series.

机构信息

Department of Paediatric Dentistry, Women's and Children's Hospital, North Adelaide, South Australia, Australia.

Adelaide Dental School, The University of Adelaide, Adelaide, South Australia, Australia.

出版信息

BMC Oral Health. 2023 Aug 18;23(1):576. doi: 10.1186/s12903-023-03275-6.

Abstract

OBJECTIVES

Molar-root incisor malformation (MRIM) is a seldom reported condition characterised by disturbances in root development of first permanent molars. This systematic review aimed to collate the clinical characteristics of individuals diagnosed with MRIM.

MATERIALS AND METHODS

A systematic search strategy using PubMed, Embase, Web of Science, and SCOPUS databases was performed through to March 2023. Inclusion criteria were case reports or case series including a diagnosis consistent with MRIM. Critical appraisal for all included studies utilised the Joanna Briggs Institute (JBI) critical appraisal checklist for case reports and case series and collation of clinical characteristics was performed in JBI System for the Unified Management, Assessment and Review of Information program.

RESULTS

The search identified 157 studies from which 35 satisfied the inclusion criteria. After full-text review, a total of 23 papers described the MRIM dental anomaly and were included in this paper. A total of 130 reported cases were retrieved, with age ranging 3-32 years, and males affected 1.16:1 females. Presence of neurological conditions, premature birth history, medication, and surgery within first years of life were synthesised and described.

CONCLUSIONS

The aetiology of MRIM is yet to be determined but epigenetic changes from significant medical history in the first years of life are likely to influence the development of this root malformation. First permanent molars were most commonly affected, but clinicians should be aware that permanent central incisors, primary teeth and other permanent teeth may also be affected.

摘要

目的

磨牙-切牙畸形(MRIM)是一种罕见的报告疾病,其特征是第一恒磨牙的牙根发育紊乱。本系统评价旨在整理诊断为 MRIM 的个体的临床特征。

材料与方法

通过 PubMed、Embase、Web of Science 和 SCOPUS 数据库进行系统搜索策略,检索截至 2023 年 3 月。纳入标准为包括符合 MRIM 诊断的病例报告或病例系列。所有纳入研究的批判性评价均采用 Joanna Briggs 研究所(JBI)病例报告和病例系列的批判性评价检查表,并在 JBI 系统中进行临床特征的整理,用于信息管理、评估和审查。

结果

搜索共确定了 157 项研究,其中 35 项符合纳入标准。经过全文审查,共有 23 篇论文描述了 MRIM 的牙齿异常,并纳入了本文。共检索到 130 例报告病例,年龄为 3-32 岁,男性和女性的发病率分别为 1.16:1 和 1.00:1。对生命头几年的神经状况、早产史、药物和手术的存在进行了综合描述。

结论

MRIM 的病因尚未确定,但生命头几年重大病史的表观遗传变化可能会影响这种牙根畸形的发育。第一恒磨牙最常受影响,但临床医生应注意,恒中切牙、乳牙和其他恒牙也可能受到影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58d6/10439578/63df61a306fc/12903_2023_3275_Fig1_HTML.jpg

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