TY - JOUR
T1 - Conjoined twins
T2 - A worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research
AU - Mutchinick, Osvaldo M.
AU - Luna-Muñoz, Leonora
AU - Amar, Emmanuelle
AU - Bakker, Marian K.
AU - Clementi, Maurizio
AU - Cocchi, Guido
AU - da Graça Dutra, Maria
AU - Feldkamp, Marcia L.
AU - Landau, Danielle
AU - Leoncini, Emanuele
AU - Li, Zhu
AU - Lowry, Brian
AU - Marengo, Lisa K.
AU - Martínez-Frías, María Luisa
AU - Mastroiacovo, Pierpaolo
AU - Métneki, Julia
AU - Morgan, Margery
AU - Pierini, Anna
AU - Rissman, Anke
AU - Ritvanen, Annukka
AU - Scarano, Gioacchino
AU - Siffel, Csaba
AU - Szabova, Elena
AU - Arteaga-Vázquez, Jazmín
PY - 2011/11/15
Y1 - 2011/11/15
N2 - 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.
AB - 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.
KW - Conjoined twins
KW - Epidemiology
KW - ICBDSR
KW - Multicentric study
UR - http://www.scopus.com/inward/record.url?scp=80054848452&partnerID=8YFLogxK
U2 - 10.1002/ajmg.c.30321
DO - 10.1002/ajmg.c.30321
M3 - Article
C2 - 22002822
AN - SCOPUS:80054848452
SN - 1552-4868
VL - 157
SP - 274
EP - 287
JO - American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
JF - American Journal of Medical Genetics, Part C: Seminars in Medical Genetics
IS - 4
ER -