Am J Perinatol 2014; 31(06): 447-454
DOI: 10.1055/s-0033-1351660
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Minor Anomalies: Can They Predict Specific Major Defects? A Study Based on 23 Major and 14 Minor Anomalies in Over 25,000 Newborns with Birth Defects

Hebe Campaña
1   Multidisciplinary Institute of Cellular Biology (IMBICE), La Plata, Argentina
,
Monica Rittler
2   Hospital Materno Infantil Ramón Sardá, University of Buenos Aires, Argentina
,
Fernando A. Poletta
3   Center for Medical Education and Clinical Research (CEMIC), Buenos Aires, Argentina
,
Juan Antonio Gili
3   Center for Medical Education and Clinical Research (CEMIC), Buenos Aires, Argentina
,
Mariela Soledad Pawluk
1   Multidisciplinary Institute of Cellular Biology (IMBICE), La Plata, Argentina
,
Sandra Constanza Scala
1   Multidisciplinary Institute of Cellular Biology (IMBICE), La Plata, Argentina
,
Jorge Santiago López Camelo
1   Multidisciplinary Institute of Cellular Biology (IMBICE), La Plata, Argentina
3   Center for Medical Education and Clinical Research (CEMIC), Buenos Aires, Argentina
› Author Affiliations
Further Information

Publication History

21 March 2013

14 June 2013

Publication Date:
21 August 2013 (online)

Abstract

Background Minor anomalies (mAs) are morphological features with little clinical relevance that have been mentioned as possible predictors of major defects (MDs).

Objectives To identify the preferential associations between selected MDs and mAs and to establish if mAs can serve as predictors for specific MDs.

Study Design Information of newborns with birth defects was obtained from the ECLAMC (Latin American Collaborative Study of Congenital Malformations) database. The sample consisted of 27,247 live- and stillborn newborns with multiple malformations that included at least one of the selected MDs or mAs. The odds ratio and predictive values were calculated for significant associations, and concurrence rates in first degree relatives.

Results  A total of 33 significant minor–major associations were identified. Single umbilical artery (SUA) and preauricular tags were the most frequent mAs; the former was associated with 10 MDs, the latter only with microtia. The highest positive predictive value was shown by SUA for anal atresia. Newborns with preauricular tags had significantly more relatives with microtia than expected.

Conclusions No new relevant associations between MDs and mAs were identified and few mAs seem to serve as predictors for specific MDs in the same newborn. However, preauricular tags can predict the occurrence of microtia in other family members.

 
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