Renal anomalies in families of individuals with congenital solitary kidney

Genetics in Medicine

Volumn 9, Issue 5, 2007, Pages 298-302

  McPherson, Elizabeth ^a  

^a MARSHFIELD CLINIC   (United States)

Author keywords

Empiric risks; Horseshoe kidney; Renal agenesis; Renal dysplasia; Solitary kidney

Indexed keywords

AGENESIS; ARTICLE; DISEASE SEVERITY; DYSPLASIA; FEMALE; HEALTH SURVEY; HUMAN; KIDNEY MALFORMATION; KIDNEY POLYCYSTIC DISEASE; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD REVIEW; QUESTIONNAIRE; RISK ASSESSMENT; SOLITARY KIDNEY; UROGENITAL TRACT MALFORMATION;

COHORT STUDIES; FAMILY; FEMALE; GENETIC COUNSELING; HUMANS; KIDNEY; KIDNEY DISEASES; MALE; QUESTIONNAIRES; RISK ASSESSMENT; UROGENITAL ABNORMALITIES; WISCONSIN;

EID: 34249059054     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e3180544516     Document Type: Article

References (20)

1. Sheih CP, Liu MB, Hung CS, Yang KH, et al. Renal abnormalities in schoolchildren. Pediatrics 1989;84:1086-1090.
2. Doroshow LW, Abeshouse BS. Congenital unilateral solitary kidney: report of 37 cases and a review of the literature. Urol Surv 1961;11:219-229.
3. Helin I, Persson PH. Prenatal diagnosis of urinary tract abnormalities by ultrasound. Pediatrics 1986;78:879-883.
4. Hiraoka M, Tsukahara H, Ohshima Y, Kasuga K, et al. Renal aplasia is the predominant cause of congenital solitary kidneys. Kidney Int 2002;61:1840-1844.
5. Bronshtein M, Bar-Hava I, Lightman A. The significance of early second-trimester sonographic detection of minor fetal renal anomalies. Prenat Diagn 1995;15:627-632.
6. Borer JG, Glassberg KI, Kassner EG, Schulsinger DA, et al. Unilateral multicystic dysplasia in 1 component of a horseshoe kidney: case reports and review of the literature. J Urol 1994;152:1568-1571.
7. Schwyzer U, Litschgi M, Schinzel A. [Familial kidney agenesis: renal adysplasia as a cause of urogenital anomalies in 3 generations]. Geburtshilfe Frauenheilkd 1989;49:759-761.
8. Krzemien G, Roszkowska-Blaim M, Kostro I, Wojnar J, et al. Urological anomalies in children with renal agenesis or multicystic dysplastic kidney. J Appl Genet 2006;47:171-176.
9. Cascio S, Paran S, Puri P. Associated urological anomalies in children with unilateral renal agenesis. J Urol 1999;162:1081-1083.
10. Thompson DP, Lynn HB. Genital anomalies associated with solitary kidney. Mayo Clin Proc 1966;41:538-548.
11. Collins DC. Congenital unilateral renal agenesis. Ann Surg 1932;95:715-726.
12. Engel D. Ueber eine seltene form der urogenitalmissbildung. Beitr Path Anat Allg Path 1920;lxvii:549-558.
13. Kolettis PN, Sandlow JI. Clinical and genetic features of patients with congenital unilateral absence of the vas deferens. Urology 2002;60:1073-1076.
14. Carter CO, Evans K, Pescia G. A family study of renal agenesis. J Med Genet 1979;16:176-188.
15. Roodhooft AM, Birnholz JC, Holmes LB. Familial nature of congenital absence and severe dysgenesis of both kidneys. N Engl J Med 1984;310:1341-1345.
16. Hilson D. Malformation of ears as sign of malformation of genito-urinary tract. BMJ 1957;2:785-789.
17. Buchta RM, Viseskul C, Gilbert EF, Sarto GE, et al. Familial bilateral renal agenesis and hereditary renal adysplasia. Z Kinderheilkd 1973;115:111-129.
18. Sanna-Cherchi S, Caridi G, Weng PL, Dagnino M, et al. Localization of a gene for non-syndromic renal hypodysplasia to chromosome 1p32-33. Am J Hum Genet 2007;80:539-549.
19. McPherson E, Carey J, Kramer A, Hall JG, et al. Dominantly inherited renal adysplasia. Am J Med Genet 1987;26:863-872.
20. Doray B, Gasser B, Reinartz I, Stoll C. Hereditary renal adysplasia in a three generations family. Genet Couns 1999;10:251-257.