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. 1984 Mar;59(3):242–245. doi: 10.1136/adc.59.3.242

Consanguinity and complex cardiac anomalies with situs ambiguus.

A R Gatrad, A P Read, G H Watson
PMCID: PMC1628545  PMID: 6712272

Abstract

A survey of British born Asian and English populations of children with congenital cardiac anomalies showed an increased incidence in the Muslim Asian population of complex lesions with visceral heterotaxia. There is a very high incidence of parental consanguinity among Muslim Asian children with complex congenital cardiac anomalies that is even higher than in the general Muslim Asian population of the area studied. The evidence suggests an important recessive genetic component in complex cardiac lesions with visceral heterotaxia, but segregation analysis does not support pure recessive inheritance.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Hurwitz R. C., Caskey C. T. Ivemark syndrome in siblings. Clin Genet. 1982 Jul;22(1):7–11. doi: 10.1111/j.1399-0004.1982.tb01402.x. [DOI] [PubMed] [Google Scholar]
  2. Jójárt G., Fekete F. P. Familiäres Asplenie-Syndrom. Acta Paediatr Acad Sci Hung. 1978;19(1):35–40. [PubMed] [Google Scholar]
  3. Li C. C., Mantel N. A simple method of estimating the segregation ratio under complete ascertainment. Am J Hum Genet. 1968 Jan;20(1):61–81. [PMC free article] [PubMed] [Google Scholar]
  4. MORTON N. E. Genetic tests under incomplete ascertainment. Am J Hum Genet. 1959 Mar;11(1):1–16. [PMC free article] [PubMed] [Google Scholar]
  5. Rose V., Izukawa T., Moës C. A. Syndromes of asplenia and polysplenia. A review of cardiac and non-cardiac malformations in 60 cases withspecial reference to diagnosis and prognosis. Br Heart J. 1975 Aug;37(8):840–852. doi: 10.1136/hrt.37.8.840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. SCHONFELD E. A., FRISCHMAN B. Syndrome of spleen agenesis, defects of the heart and vessels and situs inversus; report of a case suggesting heredity as an etiological factor. Helv Paediatr Acta. 1958 Dec;13(6):636–640. [PubMed] [Google Scholar]
  7. Wilkinson J. L., Holt P. A., Dickinson D. F., Jivani S. K. Asplenia syndrome in one of mono-zygotic twins. Eur J Cardiol. 1979 Oct;10(4):301–304. [PubMed] [Google Scholar]
  8. Zlotogora J., Elian E. Asplenia and polysplenia syndromes with abnormalities of lateralisation in a sibship. J Med Genet. 1981 Aug;18(4):301–302. doi: 10.1136/jmg.18.4.301. [DOI] [PMC free article] [PubMed] [Google Scholar]

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