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Prevalence at Birth of Cleft Lip with or without Cleft Palate: Data from the International Perinatal Database of Typical Oral Clefts (IPDTOC)
415
Citations
24
References
2010
Year
Developmental AnomalyCraniofacial DisorderGenetic EpidemiologyPediatricsCraniofacial AnomaliesMaternal HealthCleft Lip RepairBiostatisticsCleft PalateBirth Defects SurveillancePublic HealthMedicineTypical Oral CleftsEpidemiologyCleft LipBirth Defects
IPDTOC, a 2003 collaborative project funded by the NIH and WHO Human Genetics Programme, was created to study the epidemiology of craniofacial anomalies. This paper presents the prevalence of cleft lip with or without cleft palate from 54 registries in 30 countries during 2000–2005. IPDTOC gathers case‑by‑case data from EUROCAT, NBDPN, and ICBDSR registries and performs centralized analysis at ICBDSR Rome using a denominator of over 7.5 million births. Among 7,704 cases, the overall prevalence was 9.92 per 10,000 births (cleft lip 3.28, cleft lip + palate 6.64), with 76.8 % isolated, 15.9 % with other malformations, 7.3 % syndromic, and higher dysmorphological severity linked to additional system malformations.
As part of a collaborative project on the epidemiology of craniofacial anomalies, funded by the National Institutes for Dental and Craniofacial Research and channeled through the Human Genetics Programme of the World Health Organization, the International Perinatal Database of Typical Orofacial Clefts (IPDTOC) was established in 2003. IPDTOC is collecting case-by-case information on cleft lip with or without cleft palate and on cleft palate alone from birth defects registries contributing to at least one of three collaborative organizations: European Surveillance Systems of Congenital Anomalies (EUROCAT) in Europe, National Birth Defects Prevention Network (NBDPN) in the United States, and International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR) worldwide. Analysis of the collected information is performed centrally at the ICBDSR Centre in Rome, Italy, to maximize the comparability of results. The present paper, the first of a series, reports data on the prevalence of cleft lip with or without cleft palate from 54 registries in 30 countries over at least 1 complete year during the period 2000 to 2005. Thus, the denominator comprises more than 7.5 million births. A total of 7704 cases of cleft lip with or without cleft palate (7141 livebirths, 237 stillbirths, 301 terminations of pregnancy, and 25 with pregnancy outcome unknown) were available. The overall prevalence of cleft lip with or without cleft palate was 9.92 per 10,000. The prevalence of cleft lip was 3.28 per 10,000, and that of cleft lip and palate was 6.64 per 10,000. There were 5918 cases (76.8%) that were isolated, 1224 (15.9%) had malformations in other systems, and 562 (7.3%) occurred as part of recognized syndromes. Cases with greater dysmorphological severity of cleft lip with or without cleft palate were more likely to include malformations of other systems.
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