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Conte, M.L., Bertoli-Avella, A.M., de Graaf, B.M., Punzo, F., Lama, G., La Manna, A., Grassia, C., Rambaldi, P.F., Oostra, B.A. and Perrotta, S. (2008) A Genome Search for Primary Vesicoureteral Reflux Shows Further Evidence for Genetic Heterogeneity. Pediatric Nephrology, 23, 587-595.
http://dx.doi.org/10.1007/s00467-007-0675-z

has been cited by the following article:

• TITLE: Hereditary Vesicoureteral Reflux: A Study of 66 Families

  AUTHORS: Zsuzsa I. Bartik, Agneta Nordenskjöld, Sofia Sjöström, Rune Sixt, Ulla Sillén

  KEYWORDS: Vesicoureteral Reflux, Heredity, Phenotype

  JOURNAL NAME: Open Journal of Pediatrics, Vol.5 No.4, December 2, 2015

  ABSTRACT: Purpose: We studied the inheritance pattern, clinical features and outcome in children with vesicoureteral reflux (VUR). Characteristics of known familial VUR cases were also compared with those of sporadic VUR. Material and Methods: 726 patients were treated for VUR between 1990-2004. The families were contacted by letter inquiring if other members of the family were affected. The phenotype of all cases (familial and non-familial) was characterized in terms of presenting symptoms, reflux grade, recurrent urinary tract infections, kidney damage, and the natural course of reflux. Results: The response rate was 79%. A total of 99 individuals (22%) reported relatives with VUR. Since some of the 99 index cases belonged to the same family, the total number of families was ultimately 66. The distribution of relatives with VUR was: 38 siblings, 20 parents (15 mothers), 19 cousins, 15 aunts/uncles and 12 grandparents. The phenotype of VUR did not differ between familial and non-familial cases. However, VUR among relatives was of milder grade than index and sporadic cases. Conclusions: The proportion of hereditary reflux in our material was lower than in other studies (22%). We found a strong overrepresentation of maternal transmission of reflux. Severity of the disease did not differ between familial and non-familial VUR.