Complex segregation analysis of 1,792 cleft lip and palate families in South America: 1967-1997

Authors

  • Alexandre Rezende Vieira University of Iowa; Department of Pediatrics
  • Paul Anthony Romitti University of Iowa; Department of Epidemiology
  • Iêda Maria Orioli Federal University of Rio de Janeiro; Department of Genetics
  • Eduardo Enrique Castilla Oswaldo Cruz Institute; Department of Genetics

DOI:

https://doi.org/10.1590/S1517-74912003000200012

Keywords:

Cleft palate, Craniofacial abnormalities, Abnormalities, Polygenic inheritance

Abstract

Although several studies have demonstrated familial aggregation of nonsyndromic cleft lip with or without cleft palate (CL/P), its model of inheritance remains uncertain. We report the results of complex segregation analysis performed in South American families with a newborn affected with CL/P. Families of 1,792 consecutive newborns affected with CL/P and registered during the period 1967 to 1997 were studied. A model that did not include a major locus was the best-fitting model for CL/P families. This result is in agreement with previous studies which showed a significant association of several putative susceptibility loci and CL/P, indicating that the genes involved in CL/P are likely to have only a very modest impact on disease risk.

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Published

2003-06-01

Issue

Section

Patologia

How to Cite

Complex segregation analysis of 1,792 cleft lip and palate families in South America: 1967-1997. (2003). Pesquisa Odontológica Brasileira, 17(2), 161-165. https://doi.org/10.1590/S1517-74912003000200012