一名患有先天性慢性肠道假性梗阻(CIPO)儿童的磨牙釉质发育不全(MIH)

Molar Incisor Hypomineralization (MIH) in a Child with Congenital Chronic Intestinal Pseudoobstruction (CIPO).

作者信息

Zameer Mohammed, Peeran Syed Ali, Basheer Syed Nahid, Peeran Syed Wali, Birajdar Sameen Badiujjama, Alzahrani Faisal Mohammad, Alkhayrat Ali Mohammed A

机构信息

Armed Forces Hospital, Jazan, Saudi Arabia.

Department of Restorative Dentistry, College of Dentistry, Jazan, Saudi Arabia.

出版信息

Case Rep Dent. 2020 Dec 30;2020:8894657. doi: 10.1155/2020/8894657. eCollection 2020.

Abstract

Molar incisor hypomineralization (MIH) is a qualitative enamel defect of systemic origin affecting 1-4 permanent first molars (PFMs) frequently in association with affected permanent incisors (PIs). The exact etiology of MIH is still unclear but considered to be multifactorial. This present case report to the best of our knowledge is the first case reported which acknowledges MIH in a patient with chronic intestinal pseudoobstruction (CIPO) with underlying neurological disease due to somatic mitochondrial disorder. It also elicits the availability of various contemporary treatment options and their proper selection and early intervention to manage the functional and aesthetic problems caused by enamel defects and to improve the quality of life in the patients.

摘要

磨牙切牙矿化不全(MIH)是一种全身性原因导致的牙釉质质性缺陷,常影响1至4颗恒牙第一磨牙(PFMs),且常伴有受累的恒牙切牙(PIs)。MIH的确切病因仍不清楚,但被认为是多因素的。据我们所知,本病例报告是首例报道的在患有慢性肠道假性梗阻(CIPO)且因体细胞线粒体疾病存在潜在神经疾病的患者中确诊MIH的病例。它还引出了各种当代治疗方案的可用性以及对它们的正确选择和早期干预,以解决由牙釉质缺陷引起的功能和美观问题,并改善患者的生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c29/7787807/6c5a98c89539/CRID2020-8894657.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索