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Molar–incisor malformation (MIM): a case report with a comprehensive review of the literature

  • Qiang Sun1,*,†,
  • Xiaoxia Li1,†
  • Yueting Zhang2,†
  • Zhifang Wu1,*,

1Department of Pediatric Dentistry, Stomatology Hospital, School of Stomatology, Zhejiang University School of Medicine, Zhejiang Provincial Clinical Research Center for Oral Diseases, Key Laboratory of Oral Biomedical Research of Zhejiang Province, Cancer Center of Zhejiang University, Zhejiang Provincial Engineering Research Center for Oral Biomaterials and Devices, 310000 Hangzhou, Zhejiang, China

2Shaoxing Stomatological Hospital, 312500 Shaoxing, Zhejiang, China

DOI: 10.22514/jocpd.2026.107 Vol.50,Issue 4,July 2026 pp.223-232

Submitted: 23 December 2025 Accepted: 23 January 2026

Published: 03 July 2026

*Corresponding Author(s): Qiang Sun E-mail: sunqiang625@zju.edu.cn
*Corresponding Author(s): Zhifang Wu E-mail: wzf1980@zju.edu.cn

† These authors contributed equally.

Abstract

Background: Molar–incisor malformation (MIM) is a recently described dental developmental anomaly involving the first permanent molars, maxillary central incisors, and second primary molars. Reported cases remain rare worldwide, with only sporadic reports from China and other Asian populations. The condition is characterized by abnormal root development and distinctive pulp chamber alterations, posing diagnostic and therapeutic challenges in pediatric dental practice. Case: We report a case of MIM in a Chinese child presenting with apical periodontitis of a maxillary central incisor. Clinical and radiographic examinations revealed characteristic cervical enamel defects and pulp chamber calcification consistent with MIM, along with genetic findings. Microscopy-assisted root canal treatment was performed, and radiographic follow-up at 9 months demonstrated resolution of apical inflammation and satisfactory clinical outcomes. In addition, a comprehensive review of the literature on MIM published since 2014 is presented. Conclusions: This case underscores the importance of early recognition of MIM and careful differential diagnosis to avoid mismanagement. Awareness of its characteristic clinical and radiographic features can facilitate appropriate treatment planning. Further case reports and genetic studies are warranted to elucidate the etiology and optimize management strategies for affected children.


Keywords

Molar–incisor malformation; Dental developmental anomalies; Pulp calcification; Clinical management


Cite and Share

Qiang Sun,Xiaoxia Li,Yueting Zhang,Zhifang Wu. Molar–incisor malformation (MIM): a case report with a comprehensive review of the literature. Journal of Clinical Pediatric Dentistry. 2026. 50(4);223-232.

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