Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

Author:

van de Putte Romy,van Rooij Iris A. L. M.,Marcelis Carlo L. M.,Guo Michel,Brunner Han G.,Addor Marie-Claude,Cavero-Carbonell Clara,Dias Carlos M.,Draper Elizabeth S.,Etxebarriarteun Larraitz,Gatt Miriam,Haeusler Martin,Khoshnood Babak,Klungsoyr Kari,Kurinczuk Jenny J.,Lanzoni Monica,Latos-Bielenska Anna,Luyt Karen,O’Mahony Mary T.,Miller Nicola,Mullaney Carmel,Nelen Vera,Neville Amanda J.,Perthus Isabelle,Pierini Anna,Randrianaivo Hanitra,Rankin Judith,Rissmann Anke,Rouget Florence,Schaub Bruno,Tucker David,Wellesley Diana,Wiesel Awi,Zymak-Zakutnia Natalya,Loane Maria,Barisic Ingeborg,de Walle Hermien E. K.,Roeleveld Nel,Bergman Jorieke E. H.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference23 articles.

1. Quan, L. & Smith, D. W. The VATER association. Vertebral defects, anal atresia, T–E fistula with esophageal atresia, radial and renal dysplasia: a spectrum of associated defects. J. Pediatr. 82, 104–107 (1973).

2. Temtamy, S. A. & Miller, J. D. Extending the scope of the VATER association: definition of the VATER syndrome. J. Pediatr. 85, 345–349 (1974).

3. Khoury, M. J., Cordero, J. F., Greenberg, F., James, L. M. & Erickson, J. D. A population study of the VACTERL association: evidence for its etiologic heterogeneity. Pediatrics 71, 815–820 (1983).

4. EUROCAT. Prevalence Tables–Full Member Registries from 2012–2016 (2018). http://www.eurocat-network.eu/accessprevalencedata/prevalencetables . Accessed 15 Aug 2018.

5. Hilger, A. et al. Familial occurrence of the VATER/VACTERL association. Pediatr. Surg. Int. 28, 725–729 (2012).

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