当前位置： SCI文献检索 > CLEFT PALATE-CRANIOFACIAL JOURNAL期刊下所有文献 > Family-based association study of the MTHFR polymorphism C677T in patients with nonsyndromic cleft lip and palate from central Europe.

Family-based association study of the MTHFR polymorphism C677T in patients with nonsyndromic cleft lip and palate from central Europe.

Abstract：

OBJECTIVE:The 677C-->T allele in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene has been implicated in the etiology of nonsyndromic cleft lip and palate (CL/P). This study involved a family-based association study of the MTHFR polymorphism. PATIENTS/PARTICIPANTS:We examined 181 patients with CL/P of central European descent and their parents for this variant. RESULTS:The transmission disequilibrium test (TDT) did not confirm an association between the MTHFR 677C-->T polymorphism and nonsyndromic CL/P as previously suggested (p = .36). When comparing the offspring of mothers with periconceptional use of folate to those without, no statistically significant differences were found (p = .708). CONCLUSION:Our data suggest that the MTHFR 677C-->T polymorphism does not make a major contribution to the occurrence of CL/P among central Europeans.

journal_name

Cleft Palate Craniofac J

journal_title

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

authors

Reutter H,Birnbaum S,Lacava AD,Mende M,Henschke H,Bergé S,Braumann B,Lauster C,Schiefke F,Wenghoefer M,Saffar M,Reich R,Scheer M,Kramer FJ,Knapp M,Mangold E

doi

10.1597/06-174

subject

Has Abstract

pub_date

2008-05-01 00:00:00

pages

267-71

issue

3

eissn

1055-6656

issn

1545-1569

pii

06-174

journal_volume

45

pub_type

杂志文章

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