Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia

M. Goldenberg, P. Das, M. Messersmith, D. W. Stockton, P. I. Patel, R. N. D'Souza

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

A frameshift mutation recently identified within the paired domain of the transcription factor, PAXg, has been linked to a unique form of oligodontia in a single, multigenerational family (Stockton et al., 2000). We now describe the phenotypic and segregation analyses of this remarkable kindred, the initial approach taken to identify a candidate gene involved in this form of oligodontia, and the power of this single-family pedigree to generate significant linkage in a genome search. Of the 43 family members enrolled in this study, 21 individuals were affected with several congenitally missing permanent teeth. The pattern of inheritance of the oligodontia trait suggested the involvement of a single gene bearing a dominant mutation. To various degrees, affected members lacked permanent first, second, and third molars in all four quadrants. Several individuals with missing molars also lacked second premolars-most commonly, maxillary second premolars and mandibular central incisors. To the best of our knowledge, this pattern of non-syndromic, familial tooth agenesis has not been previously described in the literature. Since a missense mutation in the homeobox gene, MSX1, was previously linked to tooth agenesis in a single family lacking second premolars and third molars, we performed a mutational analysis of MSX1 by PCR. The absence of a mutation in exons 1 and 2 of MSX1 suggested that allelic mutations in the coding region of MSX1 are not associated with this phenotypically distinct form of oligodontia. Computer simulation of linkage analysis further proved that this pedigree alone was sufficient to generate a significant result for a total genome scan.

Original languageEnglish
Pages (from-to)1469-1475
Number of pages7
JournalJournal of Dental Research
Volume79
Issue number7
DOIs
StatePublished - 2000

Keywords

  • Autosomal dominance
  • Hypodontia
  • MSX1
  • Molar development
  • Oligodontia
  • Tooth agenesis

Fingerprint

Dive into the research topics of 'Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia'. Together they form a unique fingerprint.

Cite this