DLX3 mutation in a new family and its phenotypic variations.

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.

• Authors: S-K Lee, Z H Lee, S-J Lee, B-D Ahn, Y-J Kim, S-H Lee, J-W Kim
• Journal: Journal of dental research (J Dent Res) Vol. 87 Issue 4 Pg. 354-7 (Apr 2008) ISSN: 0022-0345 [Print] United States
• PMID: 18362318 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Codon
• Distal-less homeobox proteins
• Homeodomain Proteins
• Transcription Factors
• Threonine
• Cysteine

Topics

• Amelogenesis Imperfecta (genetics)
• Child
• Codon (genetics)
• Cysteine (genetics)
• Dental Enamel Hypoplasia (genetics)
• Dental Pulp Cavity (abnormalities)
• Frameshift Mutation (genetics)
• Hair (abnormalities)
• Homeodomain Proteins (genetics)
• Humans
• Male
• Nails, Malformed (genetics)
• Pedigree
• Phenotype
• Sequence Deletion (genetics)
• Syndrome
• Threonine (genetics)
• Transcription Factors (genetics)