Literature DB >> 18362318

DLX3 mutation in a new family and its phenotypic variations.

S-K Lee1, Z H Lee, S-J Lee, B-D Ahn, Y-J Kim, S-H Lee, J-W Kim.   

Abstract

Tricho-dento-osseous syndrome (TDO) is an autosomal-dominant disease characterized by curly hair at birth, enamel hypoplasia, taurodontism, and a thick cortical bone. A common DLX3 gene mutation (c.571_574delGGGG) has been identified in multiple families with variable clinical phenotypes. Recently, another DLX3 gene mutation (c.561_562delCT) was reported to cause amelogenesis imperfecta with taurodontism (AIHHT). We identified a Korean family with overlapping phenotypes of TDO and AIHHT. We performed mutational analysis to discover its genetic etiology. The identified mutation was c.561_562delCT mutation in the DLX3 gene. The enamel was hypomature and hypoplastic. The characteristic taurodontic features were not identified. Increased bone density or thickness could not be revealed by cephalometric, hand-wrist, and panoramic radiographs. Affected individuals reported that their nails were brittle, and they had curly hair at birth. This study clearly showed that the c.561_562delCT mutation had not only enamel defects, but also other clinical phenotypes resembling those of TDO syndrome.

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Year:  2008        PMID: 18362318     DOI: 10.1177/154405910808700402

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  8 in total

1.  New roles and mechanism of action of BMP4 in postnatal tooth cytodifferentiation.

Authors:  J Gluhak-Heinrich; D Guo; W Yang; M A Harris; A Lichtler; B Kream; J Zhang; J Q Feng; L C Smith; P Dechow; S E Harris
Journal:  Bone       Date:  2010-03-03       Impact factor: 4.398

2.  Neural crest deletion of Dlx3 leads to major dentin defects through down-regulation of Dspp.

Authors:  Olivier Duverger; Angela Zah; Juliane Isaac; Hong-Wei Sun; Anne K Bartels; Jane B Lian; Ariane Berdal; Joonsung Hwang; Maria I Morasso
Journal:  J Biol Chem       Date:  2012-02-20       Impact factor: 5.157

3.  Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.

Authors:  Na Zhao; Dong Han; Haochen Liu; Yue Li; Sing-Wai Wong; Zhengyi Cao; Jian Xu; Xiaowei Zhang; Tao Cai; Yixiang Wang; Hailan Feng
Journal:  Sci Rep       Date:  2016-12-07       Impact factor: 4.379

Review 4.  Amelogenesis Imperfecta; Genes, Proteins, and Pathways.

Authors:  Claire E L Smith; James A Poulter; Agne Antanaviciute; Jennifer Kirkham; Steven J Brookes; Chris F Inglehearn; Alan J Mighell
Journal:  Front Physiol       Date:  2017-06-26       Impact factor: 4.566

5.  Novel KLK4 Mutations Cause Hypomaturation Amelogenesis Imperfecta.

Authors:  Yejin Lee; Hong Zhang; Figen Seymen; Youn Jung Kim; Yelda Kasimoglu; Mine Koruyucu; James P Simmer; Jan C-C Hu; Jung-Wook Kim
Journal:  J Pers Med       Date:  2022-01-24

Review 6.  BMP Signaling Pathway in Dentin Development and Diseases.

Authors:  Mengmeng Liu; Graham Goldman; Mary MacDougall; Shuo Chen
Journal:  Cells       Date:  2022-07-16       Impact factor: 7.666

7.  Tricho-dento-osseous syndrome: diagnosis and dental management.

Authors:  Ola B Al-Batayneh
Journal:  Int J Dent       Date:  2012-08-27

8.  DLX3 interacts with GCM1 and inhibits its transactivation-stimulating activity in a homeodomain-dependent manner in human trophoblast-derived cells.

Authors:  Sha Li; Mark S Roberson
Journal:  Sci Rep       Date:  2017-05-17       Impact factor: 4.379

  8 in total

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