Please use this identifier to cite or link to this item:
https://www.arca.fiocruz.br/handle/icict/32747
Type
ArticleCopyright
Restricted access
Embargo date
2022-01-01
Collections
- IOC - Artigos de Periódicos [12654]
Metadata
Show full item record
PREFERENTIAL ASSOCIATIONS BETWEEN ORAL CLEFTS AND OTHER MAJOR CONGENITAL ANOMALIES
Author
Rittler, Monica
López-Camelo, Jorge S.
Castilla, Eduardo E.
Bermejo, Eva
Cocchi, Guido
Correa, Adolfo
Csaky-Szunyogh, Melinda
Danderfer, Ron
De Vigan, Catherine
Valle, Hermien De
Dutra, Maria da Graça
Hirahara, Fumiki
Martínez-Frias, Maria Luisa
Merlob, Paul
Mutchinick, Osvaldo
Ritvanen, Annukka
Robert-Gnansia, Elisabeth
Scarano, Gioacchino
Siffel, Csaba
Stoll, Claude
Mastroiacovo, Pierpaolo
López-Camelo, Jorge S.
Castilla, Eduardo E.
Bermejo, Eva
Cocchi, Guido
Correa, Adolfo
Csaky-Szunyogh, Melinda
Danderfer, Ron
De Vigan, Catherine
Valle, Hermien De
Dutra, Maria da Graça
Hirahara, Fumiki
Martínez-Frias, Maria Luisa
Merlob, Paul
Mutchinick, Osvaldo
Ritvanen, Annukka
Robert-Gnansia, Elisabeth
Scarano, Gioacchino
Siffel, Csaba
Stoll, Claude
Mastroiacovo, Pierpaolo
Affilliation
Hospital Materno Infantil Ramón Sardá. ECLAMC (Latin American Collaborative Study of Congenital Malformations). Buenos Aires, Argentina.
Instituto Multidisciplinario de Biología Celular (IMBICE). ECLAMC. Centro de Educación Médica e Investigación Clínica. Buenos Aires, Argentina.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Estudo Colaborativo Latinoamericano de Malformações Congênitas. Rio de Janeiro, RJ. Brasil / Centro de Educación Médica e Investigación Clínica. (CEMIC). Buenos Aires, Argentina.
Department of Epidemiology of ECEMC (Spanish Collaborative Study of Congenital Malformations). CIAC (Research Center on Congenital Anomalies, CIBERER (Center for Biomedical Research on Rare Diseases).Instituto de Salud Carlos III. Madrid, Spain.
IMER (Italy Emilia Romagna). Istituto Clinico Di Pediatria Preventiva e Neonatologia. Universitá` di Bologna. Bologna, Italy
National Center on Birth Defects and Developmental Disabilities. Centers for Disease Control and Prevention. Atlanta, Georgia, USA.
Hungarian Congenital Abnormalities Registry. Department of Human Genetics and Teratology. National Center for Epidemiology.Budapest, Hungary.
Health Status Registry. BC Vital Statistics Agency. Victoria, British Columbia, Canada.
Registre des Malformations Congénitales de Paris. INSERM U 149. Recherches Epidémiologiques en Santé Périnatale et Santé de Femmes. Villejuif, France.
EUROCAT Northern Netherlands. Department of Genetics. University Medical Center Groningen. University of Groningen. Groningen, Netherlands.
Fundação Oswaldo Cruz Fiocruz. Instituto Oswaldo Cruz. Estudo Colaborativo Latinoamericano de Malformações Congênitas. Rio de Janeiro, RJ, Brasil.
Program Director of ICBDSR Japan Center / Chair of Japan Association of Obstetricians and Gynecologists (JAOG).Professor of the Department of Obstetrics and Gynecology. Yokohama City University School of Medicine. Japan.
Director of ECEMC and CIAC. Principal Researcher of the group 724 of CIBERER. Instituto de Salud Carlos III. Madrid, Spain / Professor of the Department of Pharmacology. Faculty of Medicine. Universidad Complutense, Madrid, Spain..
Program Director (Israel? / Department of Neonatology. Rabin Medical Center. Beilinson Campus, Petah Tikva, Israel..
Program Director of RYVEMCE. Department of Genetics. National Institute of Medical Sciences / Nutrition Salvador Zubiran. Mexico City, Mexico.
Program Director (Finland). National Research and Development Centre for Welfare and Health (STAKES). Helsinki, Finland.
Program Director of REMERA. Registre de Malformations en Rhone-Alpes,. Lyon, France.
Program Director. Osservatorio Epidemiologico Regionale. Assessorato alla Sanitá. Regione Campania. Naples, Italy / Head of Medical Genetics Division. G. Rummo Hospital. Benevento, Italy.
National Center on Birth Defects and Developmental Disabilities. Centers for Disease Control and Prevention. Atlanta, Georgia.
Program Director. Professor of Medical Genetics. Laboratoire de Génétique Médicale. Faculté de Médecine. Strasbourg, France.
Director. Centre of the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR). Rome, Italy.
Instituto Multidisciplinario de Biología Celular (IMBICE). ECLAMC. Centro de Educación Médica e Investigación Clínica. Buenos Aires, Argentina.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Estudo Colaborativo Latinoamericano de Malformações Congênitas. Rio de Janeiro, RJ. Brasil / Centro de Educación Médica e Investigación Clínica. (CEMIC). Buenos Aires, Argentina.
Department of Epidemiology of ECEMC (Spanish Collaborative Study of Congenital Malformations). CIAC (Research Center on Congenital Anomalies, CIBERER (Center for Biomedical Research on Rare Diseases).Instituto de Salud Carlos III. Madrid, Spain.
IMER (Italy Emilia Romagna). Istituto Clinico Di Pediatria Preventiva e Neonatologia. Universitá` di Bologna. Bologna, Italy
National Center on Birth Defects and Developmental Disabilities. Centers for Disease Control and Prevention. Atlanta, Georgia, USA.
Hungarian Congenital Abnormalities Registry. Department of Human Genetics and Teratology. National Center for Epidemiology.Budapest, Hungary.
Health Status Registry. BC Vital Statistics Agency. Victoria, British Columbia, Canada.
Registre des Malformations Congénitales de Paris. INSERM U 149. Recherches Epidémiologiques en Santé Périnatale et Santé de Femmes. Villejuif, France.
EUROCAT Northern Netherlands. Department of Genetics. University Medical Center Groningen. University of Groningen. Groningen, Netherlands.
Fundação Oswaldo Cruz Fiocruz. Instituto Oswaldo Cruz. Estudo Colaborativo Latinoamericano de Malformações Congênitas. Rio de Janeiro, RJ, Brasil.
Program Director of ICBDSR Japan Center / Chair of Japan Association of Obstetricians and Gynecologists (JAOG).Professor of the Department of Obstetrics and Gynecology. Yokohama City University School of Medicine. Japan.
Director of ECEMC and CIAC. Principal Researcher of the group 724 of CIBERER. Instituto de Salud Carlos III. Madrid, Spain / Professor of the Department of Pharmacology. Faculty of Medicine. Universidad Complutense, Madrid, Spain..
Program Director (Israel? / Department of Neonatology. Rabin Medical Center. Beilinson Campus, Petah Tikva, Israel..
Program Director of RYVEMCE. Department of Genetics. National Institute of Medical Sciences / Nutrition Salvador Zubiran. Mexico City, Mexico.
Program Director (Finland). National Research and Development Centre for Welfare and Health (STAKES). Helsinki, Finland.
Program Director of REMERA. Registre de Malformations en Rhone-Alpes,. Lyon, France.
Program Director. Osservatorio Epidemiologico Regionale. Assessorato alla Sanitá. Regione Campania. Naples, Italy / Head of Medical Genetics Division. G. Rummo Hospital. Benevento, Italy.
National Center on Birth Defects and Developmental Disabilities. Centers for Disease Control and Prevention. Atlanta, Georgia.
Program Director. Professor of Medical Genetics. Laboratoire de Génétique Médicale. Faculté de Médecine. Strasbourg, France.
Director. Centre of the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR). Rome, Italy.
Abstract
TObjectives: To identify preferential associations between oral clefts (CL =
cleft liponly, CLP = cleft lipwith cleft palate, CP = cleft palate) and nonoral cleft anomalies, to interpret them on clinical grounds, and, based on the patterns of associated defects, to establish whether CL and CLP are different conditions. Design and Settings: Included were 1416 cleft cases (CL = 131, CLP = 565, CP = 720), among 8304 live- and stillborn infants with multiple congenital anomalies, from 6,559,028 births reported to the International Clearinghouse for Birth Defects Surveillance and Research by 15 registries between 1994 and 2004. Rates of associated anomalies were established, and multinomial logistic regressions applied to identify significant associations. Results: Positive associations with clefts were observed for only a few defects, among which anencephaly, encephaloceles, club feet, and ear anomalies were the most outstanding. Anomalies negatively associated with clefts included congenital heart defects, VATER complex (vertebral defects, imperforate anus, tracheoesophageal fistula, and radial and renal dysplasia), and spina bifida. Conclusion: The strong association between all types of clefts and
anencephaly seems to be attributable to cases with disruptions; the association between CP and club feet seems to be attributable to conditions with fetal akinesia.
Share