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Article

A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation.

Archives of oral biology - 1 Jan 2024

Quan Junkang, Liu Yang, Ji LingLi, Zhao Yuming, Zheng Shuguo

Abstract excerpt

OBJECTIVE: This study aimed to identify a DLX3 gene mutation in a family with atypical clinical manifestations of tricho-dento-osseous syndrome (TDO) and its impact on tooth enamel thickness, microhardness, structure and formation. DESIGN: Whole-exome sequencing detected DLX3 mutations in the family. Micro-CT, Vickers hardness tester, energy dispersive spectrometer and scanning electron microscopy were performed...

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Source

Identifiers

PMID: 38006713
DOI: 10.1016/j.archoralbio.2023.105849

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation.PMID 38006713Read ↗

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