| Literature DB >> 3728565 |
Abstract
Isolated, apparently nonsyndromic cleft palate (CP) is thought to be etiologically heterogeneous. The multifactorial threshold explanation for CP is postulated in most cases. Mendelian inheritance has been documented in 3 families. We report on three unrelated white families with 17 relatives in several generations affected with CP, including submucous CP and bifid/absent uvula. We could find no evidence of a cleft syndrome. In one family, the pattern is consistent with autosomal dominant inheritance. In 2 families, the pattern is consistent with X-linked recessive inheritance. The specific findings and their implications for family evaluation and genetic counseling are discussed.Entities:
Mesh:
Year: 1986 PMID: 3728565 DOI: 10.1002/ajmg.1320240309
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299