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Stuck Below: Failure of Tooth Eruption and Hereditary Enamel Defects.

作者信息

Kantaputra Piranit Nik, Sirikrai Thamon, Green Jeremy

机构信息

Center of Excellence in Medical Genetics Research, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand; Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand.

Center of Excellence in Medical Genetics Research, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand; Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Int Dent J. 2025 Aug 2;75(5):100942. doi: 10.1016/j.identj.2025.100942.

DOI:10.1016/j.identj.2025.100942
PMID:40753863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12375193/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a5/12375193/14cb8f13ecb8/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a5/12375193/14cb8f13ecb8/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a5/12375193/14cb8f13ecb8/gr1.jpg

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Stuck Below: Failure of Tooth Eruption and Hereditary Enamel Defects.下方受阻：牙齿萌出失败与遗传性牙釉质缺陷。
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本文引用的文献

1
Heimler Syndrome With Tooth Agenesis, Abnormal Enamel and Dentin Mineralization, Root Maldevelopment, and PEX1 Mutation.伴有牙齿发育不全、釉质和牙本质矿化异常、牙根发育不良及PEX1基因突变的海姆勒综合征
Int Dent J. 2025 Jun 3;75(4):100821. doi: 10.1016/j.identj.2025.04.002.
2
Abnormal dental phenotypes in GAPO syndrome: A descriptive study with a new variant & insights on teeth eruption.GAPO综合征的异常牙齿表型：一项关于新变异体的描述性研究及对牙齿萌出的见解
Saudi Dent J. 2024 Sep;36(9):1209-1214. doi: 10.1016/j.sdentj.2024.07.001. Epub 2024 Jul 2.
3
Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies.
腺瘤性结肠息肉病基因中的罕见种系变异与牙齿和骨骼异常有关。
Int J Mol Sci. 2024 Jul 26;25(15):8189. doi: 10.3390/ijms25158189.
4
Abnormal dental follicle cells: A crucial determinant in tooth eruption disorders (Review).异常的牙滤泡细胞：牙齿萌出障碍的关键决定因素（综述）。
Mol Med Rep. 2024 Sep;30(3). doi: 10.3892/mmr.2024.13292. Epub 2024 Jul 19.
5
Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta.X 连锁型牙釉质发育不全的突变与基因型-表型相关性。
Int J Mol Sci. 2024 Jun 1;25(11):6132. doi: 10.3390/ijms25116132.
6
Etiological Mechanisms and Genetic/Biological Modulation Related to PTH1R in Primary Failure of Tooth Eruption.与原发性牙萌出失败中PTH1R相关的病因机制及遗传/生物学调节
Calcif Tissue Int. 2024 Aug;115(2):101-116. doi: 10.1007/s00223-024-01227-y. Epub 2024 Jun 4.
7
A novel mutation causing amelogenesis imperfecta and its expression in human dental tissues.一种导致牙釉质发育不全的新型突变及其在人类牙齿组织中的表达。
J Dent Sci. 2024 Jan;19(1):524-531. doi: 10.1016/j.jds.2023.09.020. Epub 2023 Sep 28.
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An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature.AMELX 基因内含子 c.103-3T>C 变异导致的联合性牙本质发育不全和牙本质形成不全型：病例系列及文献复习。
Genes (Basel). 2022 Jul 18;13(7):1272. doi: 10.3390/genes13071272.
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J Appl Oral Sci. 2022 Jun 6;30:e20220028. doi: 10.1590/1678-7757-2022-0028. eCollection 2022.
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Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome.拓宽 LTBP3 变异在牙齿异常和身材矮小综合征中的基因型和表型谱。
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