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Heterotaxy: Associated conditions and hospital-based prevalence in newborns
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  • Published: 01 May 2000

Heterotaxy: Associated conditions and hospital-based prevalence in newborns

  • Angela E Lin1,2,4,
  • Baruch S Ticho3,4,
  • Kara Houde1,
  • Marie-Noel Westgate1 &
  • …
  • Lewis B Holmes1,2,4 

Genetics in Medicine volume 2, pages 157–172 (2000)Cite this article

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Abstract

Purpose: To provide insight into the possible etiology and prevalence of heterotaxy, we studied conditions associated with heterotaxy in a consecutive hospital population of newborns.

Methods: From 1972 to March, 1999 (except February 16, 1972 to December 31, 1978), 58 cases of heterotaxy were ascertained from a cohort of 201,084 births in the ongoing Active Malformation Surveillance Program at the Brigham and Women's Hospital. This registry includes livebirths, stillbirths, and elective abortions. Prevalence among nontransfers (i.e., patients whose mothers had planned delivery at this hospital) was calculated as approximately 1 per 10,000 total births (20 of 201,084).

Results: We analyzed a total of 58 patients consisting of 20 (34%) nontransfers and 38 (66%) transfers. Patients were categorized by spleen status as having asplenia (7 nontransfers, 25 total), polysplenia (8, 20), right spleen (4, 11), normal left (0, 1), and unknown (1, 0). Among the 20 nontransfer and 59 total heterotaxy patients, the following associated medical conditions were present: chromosome abnormality (1 nontransfer, 2 total), suspected Mendelian or chromosome microdeletion disorder (1 nontransfer, 6 total), and maternal insulin-dependent diabetes mellitus (1 nontransfer, 2 total). There were 6 twins (1 member each from 6 twin pairs including 1 dizygous, 4 monozygous, 1 conjoined; 2 were nontransfers). An associated condition occurred in 5 (25%) nontransfer and 16 (28%) total patients, or among 10 of 53 singleton births (19%).

Conclusions: Although most cases of heterotaxy in this series were sporadic events, an associated condition was present in about one-fourth of the cases. Not all of these conditions would be considered causative etiologies. Based on this small series alone, maternal insulin-dependent diabetes cannot be viewed as a risk factor for heterotaxy. However, the specific association of diabetes with polysplenia with/without left atrial isomerism is noteworthy, and adds weight to animal and epidemiologic case-control data.

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Authors and Affiliations

  1. Department of Newborn Medicine, the Brigham and Women's Hospital, Boston, Massachusetts

    Angela E Lin, Kara Houde, Marie-Noel Westgate & Lewis B Holmes

  2. Genetics and Teratology Unit, Pediatric Service, Boston, Massachusetts

    Angela E Lin & Lewis B Holmes

  3. Division of Pediatric Cardiology, Massachusetts General Hospital, Boston, Massachusetts

    Baruch S Ticho

  4. Department of Pediatrics, Harvard Medical School, Boston, Massachusetts

    Angela E Lin, Baruch S Ticho & Lewis B Holmes

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  1. Angela E Lin
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  2. Baruch S Ticho
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  3. Kara Houde
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Lin, A., Ticho, B., Houde, K. et al. Heterotaxy: Associated conditions and hospital-based prevalence in newborns. Genet Med 2, 157–172 (2000). https://doi.org/10.1097/00125817-200005000-00002

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  • Received: 21 February 2000

  • Accepted: 24 March 2000

  • Issue date: 01 May 2000

  • DOI: https://doi.org/10.1097/00125817-200005000-00002

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Keywords

  • Asplenia
  • cardiovascular malformations
  • congenital heart defects
  • defects of right
  • left determination
  • genetic epidemiology
  • heterotaxy
  • isomerism
  • laterality defects
  • maternal diabetes
  • polysplenia
  • prevalence
  • situs ambiguous
  • situs inversus

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Genetics in Medicine (Genet Med)

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ISSN 1098-3600 (print)

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