Molecular basis of vesicoureteral reflux;Le basi molecolari del reflusso vescico-ureterale

Minerva Pediatrica

Volumn 54, Issue 5, 2002, Pages 415-422

  Lama, G ^a   Salsano, M Esposito ^a  

^a SECOND UNIVERSITY OF NAPLES   (Italy)

Author keywords

Vesico ureteral reflux, congenital; Vesico ureteral reflux, diagnosis; Vesico ureteral reflux, genetics

Indexed keywords

CHILD; GENETICS; HUMAN; REVIEW; VESICOURETERAL REFLUX;

CHILD; HUMANS; VESICO-URETERAL REFLUX;

EID: 0036778441     PISSN: 00264946     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (56)

1. Peters PC, Johnson DE, Jakson JH. The incidence of vesicoureteral reflux in the premature child. J Urol 1967;97:259-65.
2. Bailey RR. Vesicoureteric reflux in healthy infants and children. In: Hodson J, Kincaid-Smith P, editors. Reflux nephropathy. Masson: New York; 1975. p. 59-61.
3. Miller HC, Caspari EW. Ureteral reflux as genetic trait. J Am Med Assoc 1972;220:842-3.
4. Bredin HC, Winchester P, McGovern JH, Degnian M. Family study of vesico-ureteral reflux. J Urol 1975;113 623-5.
5. De Vargas A, Evans K, Ransley P, Rosenberg AR. Rothwell D, Sherwood T et al. A family study of vesico-ureteric reflux. J Genet 1978;15:85-96.
6. Jerkins GR, Noe HN. Familial vesico-ureteral reflux: a prospective study. J Urol 1982;128:774-8.
7. Noe HN, Wyatt RJ, Peedeen JN Jr, Rivas ML. The trasmission of vesico-ureteral reflux from parent to child J Urol 1992;148:1869-71.
8. Van den Abbeele AD, Treves ST, Lebowitz RL, Bauer S. Davis NMT, Retick A et al. Vesico-ureteral reflux in asymptomatic siblings of patient with known reflux: radionuclide cystography. Pediatrics 1987;79:147-53.
9. Noe HN. The long term results of prospective sibling reflux screening. J Urol 1992;148:1739-42.
10. Kaefer M, Curran M, Treves T, Bauer S, Hendren WH, CA Peters et al. Sibling vesicoureteral reflux in multiple gestation births. Pediatrics 2000;105:800-4.
11. Feather S, Woolf AS, Gordon I, Risdon RA, Verrier Jones K. Vesicoureteric reflux: is it all in the genes? Lancet 1996;348:725-8.
12. Smellie JM, Prescod N. Natural history of overt urinary tract infection childhood. In: Asscher AA, Brumfitt W, editors. Microbial disease in nephrology. Chichester, UK: Wiley; 1986. p. 243-60.
13. Ransley PG, Risdon RA, Gedley ML. High pressare, sterile vesicoureteral reflux and renal scarring: an experimental study in the pig and minipig. Contrib Nephrol 1984;39:320-43.
14. Risdon RA, Yeung CK, Ransley P. Reflux nephropathy in children submitted to nephrectomy: a clinicopathological study. Clin Nephrol 1993;40:308-14.
15. Ransley PG, Risdon RA. Reflux and renal scarring. Br J Radiol 1978;14:1-35.
16. Bailey RR, Lynn KL, Robson RO. End stage reflux nephropathy. Renal Failure 1994;16:27-35.
17. Zhang Y, Bailey RR. Long tern follow-up of adults with reflux nephropathy. N Z Med J 1995;108:142-4.
18. Kincaid-Smith PS, Bastos MG, Becker GJ. Reflux nephropathy in the adult. Contrib Nephrol 1984;39:94-9.
19. Hinchliffe SS, Chan YF, Jones H, Kreczy JP, Van Velzen D. Renal hypoplasia and postnatal acquired cortical loss in children with vesicoureteral reflux. Pediatr Nephrol 1992;6:439-44.
20. Cook WA, Stephens FD. Congenital urologie anomalies. In: Schrier RW, Gottschalk CW, editors. Disease of the kidney. Boston: Little Brown and Company; 1983;1. p. 637-55.
21. Tucker K, Lipson A. Choanal atresia as a feature of ectrodactyly-ectodermal displasia-clefting (EEC) syndrome: a further case. J Med Genet 1990;27:213.
22. Schimmenti LA, Pierpont ME, Carpenter BLM, Kashtan CE, Johnson MR, Dobyn WB. Autosomal dominant optic nerve colobomas, vesicoureteral reflux and renal anomalies. Am J Med Genet 1995;59:204-8.
23. Hain MD, Winter RM, Burn J. Robinow sindrome without mesomelic brachymelia: a report of five case. J Med Genet 1986;23:350-4.
24. Fisher AM, Barber JC, Crolla JA, James RS, Lestas AN, Jennings J et al. Mosaic tetrasomy 8p: molecular cytogentic confirmation and measurement of glutathione reductase and tissue plasminogen activator levels. Am J Med Genet 1993;47:100-5.
25. Chapman HE, Gunn TR. Family with partial monosomy 10p and trisomy 10p. Am J Med Genet 1995;56:136-40.
26. Scott JES, Swallow V, Coulthard MG, Lambert HJ, Lee REJ. Screening of newborn babies for familial ureteric reflux. Lancet 1997;350:396-400.
27. Aggarwal VK, Verrier Jones K. Vesicoureteric reflux: screening of first degree relatives. Arch Dis Child 1989;64:1538-41.
28. Chapman CJ, Bailey RR, Janus ED, Abbott GD, Lynn KL. Vesicoureteral reflux: segregation analysis. Am J Genet 1985;20:577-84.
29. Rocco G, Esposito Salsano M, Avino G, De Rosa C, Luongo I, Lama G. Reflusso vescico-ureterale e familiarità. RIP 1997;23 Suppl 4:116.
30. Bailey RR, Fallace M. HLA-B12 as a genetic marker for vesicoureteral reflux? Br Med 1978;1:48-9.
31. Sengar DPS, McLeish WA, Rashid A, Wolfish NM. Histocompatibility antigens in urinary tract infection and vesicoureteral reflux, a preliminary communication Clin Nephrol 1978;10:166-9.
32. Middleton GW, Howards SS, Gillenwater JY. Sex-linked familial reflux. J Urol 1975;114:36-9.
33. Macintosh M, Almarhoos G, Heath DA. HLA linkage with familial vesicoureteral reflux and familial pelviureteric junction obstruction. Tissue Antig 1989;34:185-9.
34. Klemme LA, Fish AJ, Rich S, Greenberg B, Senske B, Segall M. Familial ureteral abnormalities syndrome: genomic mapping, clinical findings. Pediatr Nephrol 1998;12:349-56.
35. Sanyanusin P, Schimraenti LA, McNoe LA, Ward TA, Pierpoint MEM, Sullivan MJ et al. Mutations of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Nat Genet 1995;9:358-64.
36. Eccles MR, Bailey RR, Abbott GD, Sullivan MJ. Unravelling the genetics of vesicoureteric reflux: a common familial disorder. Hum Mol Gen 1996;5:1425-9.
37. Schuchardt A, D'Agati V, Pachnis V, Costantini F. Renal agenesis and hypodysplasia in ret-k-mutant mice result from defects in ureteric bud development. Development 1996;122:1919-29.
38. Nishimura H, Yerkes E, Hohenfeller K, Miyazaki Y, Ma JH, Yoshida Ichiki T et al. Role of the angiotensin type receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men. Mol Cell 1999;3:1-10.
39. Hohenfeller K, Huntley TF, Shloemer C, Brenner W, Yerkes H, Zepp F et al. Angiotensin type 2 receptor is important in the normal development of the ureter. Pediatr Nephrol 1999;13:187-91.
40. Ping Hu, Fang Ming Deng, Feng Xia-Lang, Chuan-Min Hu, Auerbach AB, Shapiro E et al. Ablation of Uroplakin III gene results in small Urothelial Plaques, Urothelial Leakage, and Vesicouretersl Reflux. J Cell Biol 2000;151(5):961-71.
41. Feather SA, Malcolm S, Woolf AS, Vright V, Blaydon D, Reid CJD et al. Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1. Am J Hum Genet 2000;66:1420-5.
42. Vainio S, Muller U. Inductive tissue interactions, cell signaling, and the control of kidney organogenesis. Cell 1997;90:975-8.
43. th ed. Baltimore: William & Wilkins; 1999. p. 1-19.
44. Eccles MR. The role of PAX2 in normal and abnormal development of the urinary tract. Pediatr Nephrol 1998;12:712-20.
45. Risdon RA, Woolf AS. Development defects and cystic diseases of the kidney. Heptinstall's Patol Kidney 1998: :1149-206.
46. Sanyanusin P, McNoe LA, Sullivan MJ, Weaver RG, Eccles MR. Mutation of PAX2 in two siblings with renal-coloboma syndrome Hum Mol Genet 1995;4:2183-4.
47. Perrotta S, Russo M, Grassia C, Di Pinto D, Rocco G, Esposito Salsano M, Lama G. The role of PAX2 gene mutations in patients with hereditary vesicoureteric reflux. Pediatr Nephiol 2000;6:C52.
48. Hardelin JP, Juillard AK, Moniot B, Yanicostas N, Verney C, Schwanzel-Fukucla M et al. Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the development anomalies of X chromosome-linked Kallmann syndrome. Rev Dyn 1999;215: 26-44.
49. Yamada T, Horiuchi VJ, Dzau VJ. Angiotensin II type 2 receptor mediates programmed cell death. Proc Natl Acad Sci USA 1996;93:156-60.
50. Miyazaki Y, Tushida S, Nishimura H, Pope JC IV, Harris RC, McKanna JM et al. Angiotensin induces the urinary peristaltic machinery during the perinatal period. J Clin Invest 1998;102:1489-97.
51. Wu XR, Lin JH, Walz JT, Haner JM, Yu JJ, Aebi U et al. Mammalian uroplakins. A group of highly conserved urothelial differentation-related membrane proteins. J Biol Chem 1994;269:13716-24.
52. Finch JL, Webb GC, Evdokiou A, Cowled PA. Chromosomal localization of the human urothelial "tetraspan" gene, UPKIB, to 3q 13.3-q21 and detection of a Taq1 polymorphism. Genomics 1997;40:501-3.
53. Kitayama H, Sugimoto Y, Matsuzaki T, Ikawa Y, Noca M. A ras-related gene with transformation suppressor activity. Cell 1989;56:77-84.
54. Madaule P, Axel R A novel ras-related gene family. Cell 1985;41:31-40.
55. Wada T, Naito T, Griffiths RC, Coffman TM, Kelley VR. Systemic autoimmune nephritogenic components induce CSF-1 and TNF-alfa in MRL kidneys. Kidney Int 1997;53:934-41.
56. Devriendt K, Groenen P, Van Esch H, van Dijck M, Van de Ven W, Fryns JP et al. Velico-ureteral reflux: a genetic condition? Eur J Pediatr 1998;157:265-71.