Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research.

Osvaldo M Mutchinick, Leonora Luna-Muñoz, Emmanuelle Amar, Marian K Bakker, Maurizio Clementi, Guido Cocchi, Maria da Graça Dutra, Marcia L Feldkamp, Danielle Landau, Emanuele Leoncini, Zhu Li, Brian Lowry, Lisa K Marengo, María-Luisa Martínez-Frías, Pierpaolo Mastroiacovo, Julia Métneki, Margery Morgan, Anna Pierini, Anke Rissman, Annukka Ritvanen, Gioacchino Scarano, Csaba Siffel, Elena Szabova, Jazmín Arteaga-Vázquez

Journal: American journal of medical genetics. Part C, Seminars in medical genetics 2012;157C(4):274-87

PMID: 22002822

Abstract

Conjoined twins (CT) are a very rare developmental accident of uncertain etiology. Prevalence has been previously estimated to be 1 in 50,000 to 1 in 100,000 births. The process by which monozygotic twins do not fully separate but form CT is not well understood. The purpose of the present study was to analyze diverse epidemiological aspects of CT, including the different variables listed in the Introduction Section of this issue of the Journal. The study was made possible using the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR) structure. This multicenter worldwide research includes the largest sample of CT ever studied. A total of 383 carefully reviewed sets of CT obtained from 26,138,837 births reported by 21 Clearinghouse Surveillance Programs (SP) were included in the analysis. Total prevalence was 1.47 per 100,000 births (95% CI: 1.32-1.62). Salient findings including an evident variation in prevalence among SPs: a marked variation in the type of pregnancy outcome, a similarity in the proportion of CT types among programs: a significant female predominance in CT: particularly of the thoracopagus type and a significant male predominance in parapagus and parasitic types: significant differences in prevalence by ethnicity and an apparent increasing prevalence trend in South American countries. No genetic, environmental or demographic significant associated factors were identified. Further work in epidemiology and molecular research is necessary to understand the etiology and pathogenesis involved in the development of this fascinating phenomenon of nature.

Copyright © 2011 Wiley Periodicals, Inc.

Address: Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán", Departamento de Genética, Registro y Vigilancia Epidemiológica de Malformaciones Congénitas, México City, Mexico. [email protected]
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.