Long-term trends in the prevalence of congenital heart defects in patients with down syndrome in southern Poland

1Lejeune J, Gautier M, Turpin R. [Study of somatic chromosomes from 9 mongoloid children]. [Article in French]. CR Hebd Seances Acad Sci. 1959;248(11):17211722.Lejeune J Gautier M Turpin R [Study of somatic chromosomes from 9 mongoloid children]. [Article in French] CR Hebd Seances Acad Sci 19592481117211722Search in Google Scholar

2Coppedè F. Risk factors for Down syndrome. Arch Toxicol. 2016;90(12):2917-2929. doi: 10.1007/s00204-016-1843-3.Coppedè F Risk factors for Down syndrome Arch Toxicol 201690122917 2929 10.1007/s00204-016-1843-327600794Open DOISearch in Google Scholar

3Ghosh S, Feingold E, Dey SK. Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations. Am J Med Genet A. 2009;149A(7):1415-1420. doi: 10.1002/ajmg.a.32932.Ghosh S Feingold E Dey SK Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations Am J Med Genet A 2009149A71415 1420 10.1002/ajmg.a.32932273274919533770Open DOISearch in Google Scholar

4Yoon PW, Freeman SB, Sherman SL, Taft LF, Gu Y, Pettay D, Flanders WD, Khoury MJ, Hassold TJ. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. Am J Hum Genet. 1996;58(3):628-633.Yoon PW Freeman SB Sherman SL Taft LF Gu Y Pettay D Flanders WD Khoury MJ Hassold TJ Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study Am J Hum Genet 1996583628 633Search in Google Scholar

5Ballesta F, Queralt R, Gómez D, Solsona E, Guitart M, Ezquerra M, Moreno J, Oliva R. Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21. Ann Genet. 1999;42(1):11-15.Ballesta F Queralt R Gómez D Solsona E Guitart M Ezquerra M Moreno J Oliva R Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21 Ann Genet 199942111 15Search in Google Scholar

6Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL, Watkins PC, Metaxotou C, Antonarakis SE. Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome. Science. 1987;237(4815):652-654. doi: 10.1126/science.2955519.Warren AC Chakravarti A Wong C Slaugenhaupt SA Halloran SL Watkins PC Metaxotou C Antonarakis SE Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome Science 19872374815652 654 10.1126/science.29555192955519Open DOISearch in Google Scholar

7Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum Mol Genet. 1997;6(9):1391-1399. doi: 10.1093/hmg/6.9.1391.Lamb NE Feingold E Savage A Avramopoulos D Freeman S Gu Y Hallberg A Hersey J Karadima G Pettay D Saker D Shen J Taft L Mikkelsen M Petersen MB Hassold T Sherman SL Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21 Hum Mol Genet 1997691391 1399 10.1093/hmg/6.9.13919285774Open DOISearch in Google Scholar

8Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SL. Association between maternal age and meiotic recombination for trisomy 21. Am J Hum Genet. 2005;76(1):91-99. doi: 10.1086/427266.Lamb NE Yu K Shaffer J Feingold E Sherman SL Association between maternal age and meiotic recombination for trisomy 21 Am J Hum Genet 200576191 99 10.1086/427266119643715551222Open DOISearch in Google Scholar

9Flores-Ramírez F, Palacios-Guerrero C, García-Delgado C, Morales-Jiménez AB, Arias-Villegas CM, Cervantes A, Morán-Barroso VF. Cytogenetic profile in 1,921 cases of trisomy 21 syndrome. Arch Med Res. 2015;46(6):484-489. doi: 10.1016/j.arcmed.2015.08.001.Flores-Ramírez F Palacios-Guerrero C García-Delgado C Morales-Jiménez AB Arias-Villegas CM Cervantes A Morán-Barroso VF Cytogenetic profile in 1,921 cases of trisomy 21 syndrome Arch Med Res 2015466484 489 10.1016/j.arcmed.2015.08.00126314225Open DOISearch in Google Scholar

10Morris JK, Alberman E, Mutton D, Jacobs P. Cytogenetic and epidemiological findings in Down syndrome: England and Wales 1989-2009. Am J Med Genet A. 2012;158A(5):1151-1157. doi: 10.1002/ajmg.a.35248.Morris JK Alberman E Mutton D Jacobs P Cytogenetic and epidemiological findings in Down syndrome: England and Wales 1989-2009 Am J Med Genet A 2012158A51151 1157 10.1002/ajmg.a.3524822438132Open DOISearch in Google Scholar

11Stoll C, Dott B, Alembik Y, Roth MP. Associated congenital anomalies among cases with Down syndrome. Eur J Med Genet. 2015;58(12):674-680. doi: 10.1016/j.ejmg.2015.11.003.Stoll C Dott B Alembik Y Roth MP Associated congenital anomalies among cases with Down syndrome Eur J Med Genet 20155812674 680 10.1016/j.ejmg.2015.11.00326578241Open DOISearch in Google Scholar

12Konik R, Pietrzyk JJ. [Congenital anomalies of the developmental age. I. Incidence of malformations in newborn infants diagnosed the 1st week of life in the Cracow Region]. [Article in Polish]. Pediatr Pol. 1976;51(10):1157-1162.Konik R Pietrzyk JJ [Congenital anomalies of the developmental age. I. Incidence of malformations in newborn infants diagnosed the 1st week of life in the Cracow Region]. [Article in Polish] Pediatr Pol 197651101157 1162Search in Google Scholar

13Malec E, Mroczek T, Pajak J, Januszewska K, Zdebska E. Results of surgical treatment of congenital heart defects in children with Down’s syndrome. Pediatr Cardiol. 1999;20(5):351-354. doi: 10.1007/s002469900483.Malec E Mroczek T Pajak J Januszewska K Zdebska E Results of surgical treatment of congenital heart defects in children with Down’s syndrome Pediatr Cardiol 1999205351 354 10.1007/s00246990048310441690Open DOISearch in Google Scholar