Authors:
ABSTRACT
Aim
Tooth agenesis is characterised by the congenital absence of one or more teeth. The Pax9 gene has been
associated with nonsyndromic forms.
Methods
To investigate the molecular mechanisms, we evaluated
specific haplotypes frequency in exon 3 of the Pax9 gene in 26 patients and 21 controls, using an Italian population.
Results
Presence of His239His and the Ala240Pro were confirmed in exon 3 of the Pax9 gene. A frequency of 20.2
of the T allele at position 717 and a C frequency of 33 of Ala240Pro polymorphism, that reached 40.5 in the
control group, were observed. The 39 C/C-240 C/C or G/Chaplotype which we defined Pax9hapl a had a proportion of
61.9 in control individuals. The frequency of Pax9hapl a tested in the patients was different from controls, being
81.3 in normalcy and 18.8 in oligodontia (p<0.05).
Conclusion
Our observations suggest that Pax9hapl a
may have a protective effect against sporadic oligodontia.
PLUMX METRICS
Publication date:
Keywords:
Issue:
Vol.12 – n.4/2011
Page:
Publisher:
Cite:
Harvard: C. Arcuri, I. Zito, F. Santini, F. Muzzi, V. Panetta, R. Squitti (2011) "Understanding the implications of the PAX9 Gene in tooth development", European Journal of Paediatric Dentistry, 12(4), pp245-248. doi:
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