Prevalence of orofacial clefts in Korean live births
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Objective The aim of this study was to investigate the prevalence of orofacial clefts and identify the characteristics of other birth defects associated with orofacial clefts in Korea. Methods This study used data from the Congenital Anomaly Survey conducted by the Korea Institute for Health and Social Affairs. The survey was conducted on birth defects documented during 2005 to 2006 in 2,348 medical institutes in Korea. This study was performed using data from medical insurance claims of the National Health Insurance Corporation. The prevalence of orofacial clefts was defined as the number of cases per 10,000 live births. Results Among the 883,184 live births, 25,335 infants had birth defects, which included 980 infants with orofacial clefts. The prevalence of total orofacial clefts in the total live births was 11.09 per 10,000, accounting for 3.9% of all birth defects. The most common orofacial cleft was cleft palate only (n=492), followed by cleft lip only (n=245) and cleft lip with cleft palate (n=243), with prevalence rates of 5.57, 2.77, 2.75 per 10,000 live births, respectively. While malformations of the circulatory system; digestive system; eyes, ears, face, and neck; and musculoskeletal system were most frequently encountered among infants with a cleft lip with or without a cleft palate, anomalies of most organ systems were notably observed among infants with cleft palate only. Conclusion The prevalence of orofacial clefts in Korea was similar or slightly lower than that of other countries. This study informs present status of orofacial clefts and gives baseline data to lay the foundation stone for Korea’s registry system of orofacial clefts.
Abstract
Objective The aim of this study was to investigate the prevalence of orofacial clefts and identify the characteristics of other birth defects associated with orofacial clefts in Korea. Methods This study used data from the Congenital Anomaly Survey conducted by the Korea Institute for Health and Social Affairs. The survey was conducted on birth defects documented during 2005 to 2006 in 2,348 medical institutes in Korea. This study was performed using data from medical insurance claims of the National Health Insurance Corporation. The prevalence of orofacial clefts was defined as the number of cases per 10,000 live births. Results Among the 883,184 live births, 25,335 infants had birth defects, which included 980 infants with orofacial clefts. The prevalence of total orofacial clefts in the total live births was 11.09 per 10,000, accounting for 3.9% of all birth defects. The most common orofacial cleft was cleft palate only (n=492), followed by cleft lip only (n=245) and cleft lip with cleft palate (n=243), with prevalence rates of 5.57, 2.77, 2.75 per 10,000 live births, respectively. While malformations of the circulatory system; digestive system; eyes, ears, face, and neck; and musculoskeletal system were most frequently encountered among infants with a cleft lip with or without a cleft palate, anomalies of most organ systems were notably observed among infants with cleft palate only. Conclusion The prevalence of orofacial clefts in Korea was similar or slightly lower than that of other countries. This study informs present status of orofacial clefts and gives baseline data to lay the foundation stone for Korea’s registry system of orofacial clefts.
참고문헌 (17)
- Canfield MA., "National estimates and race", ethnicspecific variation of selected birth defects in the United States, 1999-2001, 2006, pp.76, 747~756
- Murray JC., "Gene", environment causes of cleft lip and, Clin Genet, pp.2002, 61[DOI]
- Spritz RA., "The genetics and epigenetics of orofacial clefts", Curr Opin Pediatr, 13, pp.556~560 (2001)
- Sarkozi A., "Oral clefts with associated anomalies : findings in the Hungarian Congenital Abnormality Registry", BMC Oral Health, 5, pp.4~ (2005)
- Derijcke A., "The incidence of oral clefts : a review", Br J Oral Maxillofac Surg, 34, pp.488~494 (1996)
- "The epidemiology of cleft lip and palate in Canada, 1998 to 2007"[URL]
- Genisca AE., "Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004", Am J Med Genet A, 149A, pp.1149~1158 (2009)
- Fraser FC., "The genetics of cleft lip and cleft palate", Am J Hum Genet, 22, pp.336~352 (1970)
- Shaw GM., "Congenital malformations in births with orofacial clefts among 3.6 million California births, 1983-1997", Am J Med Genet A, 125A, pp.250~256 (2004)
- Milerad J., "Associated malformations in infants with cleft lip and palate: a prospective, population-based study", Pediatrics, 100(2 Pt 1), pp.180~186 (1997)
- Shafi T., "Congenital heart disease and associated malformations in children with cleft lip and palate in Pakistan", Br J Plast Surg, 56, pp.106~109 (2003)
- Shprintzen RJ., "Anomalies associated with cleft lip, cleft palate, or both", Am J Med Genet, 20, pp.585~595 (1985)
- Vallino-Napoli LD., "An epidemiologic study of orofacial clefts with other birth defects in Victoria, Australia", Cleft Palate Craniofac J, 43, pp.571~576 (2006)
- Van der Veen FJ., "Regional underreporting of associated congenital anomalies in cleft patients in the Netherlands", Cleft Palate Craniofac J, 43, pp.710~714 (2006)
- Wyse RK., "Congenital heart anomalies in patients with clefts of the lip and", or palate, 1990, pp.27, 258~264
- Knox EG, "Epidemiology of congenital malformations" (1991), Her Mejesty’s Stationary Office
- Cordero JF., "Finding the causes of birth defects", N Engl J Med, 331, pp.48~49 (1994)
