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Volumn 27, Issue 6, 2012, Pages 965-972

Early risk factors for neonatal mortality in CAKUT: Analysis of 524 affected newborns

Author keywords

Fetal hydronephrosis; Prenatal diagnosis; Prevalence; Renal agenesis; Renal cystic disease; Urinary tract malformations

Indexed keywords

AMNION FLUID; ARTICLE; AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE; CHROMOSOME 4; CHROMOSOME ABERRATION; CONGENITAL ABNORMALITY OF THE KIDNEY AND URINARY TRACT; CONGENITAL MALFORMATION; ECTOPIC KIDNEY; FEMALE; FETAL HYDANTOIN SYNDROME; FETUS ECHOGRAPHY; HORSESHOE KIDNEY; HOSPITALIZATION; HUMAN; HYPOPLASTIC BLADDER; HYPOSPADIAS; ISOLATED HYDRONEPHROSIS; KIDNEY AGENESIS; KIDNEY DISEASE; KIDNEY PARENCHYMA; KIDNEY POLYCYSTIC DISEASE; LIVE BIRTH; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; MEGABLADDER; MEGAURETER; MULTICYSTIC DYSPLASTIC KIDNEY; NEWBORN; NEWBORN MORTALITY; OLIGOHYDRAMNIOS; PARTIAL TRISOMY 9; PREGNANCY; PREMATURITY; PRIORITY JOURNAL; RENAL CYST IN SYNDROME; RENAL HYPODYSPLASIA; RENAL SIMPLE CYST; RISK FACTOR; TERTIARY HEALTH CARE; TRISOMY 18; TRISOMY 21; URETHRA ATRESIA; URINARY TRACT DILATATION; URINARY TRACT MALFORMATION;

EID: 84863984854     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-012-2107-y     Document Type: Article
Times cited : (74)

References (49)
  • 1
    • 77957253564 scopus 로고    scopus 로고
    • Renal malformations associated with mutations of developmental genes: Messages from the clinic
    • Adalat S, Bockenhauer D, Ledermann SE, Hennekam RC, Woolf AS (2010) Renal malformations associated with mutations of developmental genes: messages from the clinic. Pediatr Nephrol 25:2247-2255
    • (2010) Pediatr Nephrol , vol.25 , pp. 2247-2255
    • Adalat, S.1    Bockenhauer, D.2    Ledermann, S.E.3    Hennekam, R.C.4    Woolf, A.S.5
  • 3
    • 65949095717 scopus 로고    scopus 로고
    • Genetic and developmental basis for urinary tract obstruction
    • Chen F (2009) Genetic and developmental basis for urinary tract obstruction. Pediatr Nephrol 24:1621-1632
    • (2009) Pediatr Nephrol , vol.24 , pp. 1621-1632
    • Chen, F.1
  • 4
    • 77951255293 scopus 로고    scopus 로고
    • Urinary levels of interleukin-6 and interleukin-8 in patients with vesicoureteral reflux and renal parenchymal scar
    • Gokce I, Alpay H, Biyikli N, Unluguzel G, Dede F, Topuzoglu A (2010) Urinary levels of interleukin-6 and interleukin-8 in patients with vesicoureteral reflux and renal parenchymal scar. Pediatr Nephrol 25:905-912
    • (2010) Pediatr Nephrol , vol.25 , pp. 905-912
    • Gokce, I.1    Alpay, H.2    Biyikli, N.3    Unluguzel, G.4    Dede, F.5    Topuzoglu, A.6
  • 5
    • 77955013992 scopus 로고    scopus 로고
    • Antenatal and postnatal ultrasound in the evaluation of the risk of vesicoureteral reflux
    • Grazioli S, Parvex P, Merlini L, Combescure C, Girardin E (2010) Antenatal and postnatal ultrasound in the evaluation of the risk of vesicoureteral reflux. Pediatr Nephrol 25:1687-1692
    • (2010) Pediatr Nephrol , vol.25 , pp. 1687-1692
    • Grazioli, S.1    Parvex, P.2    Merlini, L.3    Combescure, C.4    Girardin, E.5
  • 6
    • 77951259153 scopus 로고    scopus 로고
    • Molecular anatomy of the kidney: What have we learned from gene expression and functional genomics?
    • Rumballe B, Georgas K, Wilkinson L, Little M (2010) Molecular anatomy of the kidney: what have we learned from gene expression and functional genomics? Pediatr Nephrol 25:1005-1016
    • (2010) Pediatr Nephrol , vol.25 , pp. 1005-1016
    • Rumballe, B.1    Georgas, K.2    Wilkinson, L.3    Little, M.4
  • 7
    • 79955034410 scopus 로고    scopus 로고
    • Genetics of congenital anomalies of the kidney and urinary tract
    • Song R, Yosypiv IV (2011) Genetics of congenital anomalies of the kidney and urinary tract. Pediatr Nephrol 26:353-364
    • (2011) Pediatr Nephrol , vol.26 , pp. 353-364
    • Song, R.1    Yosypiv, I.V.2
  • 10
    • 0034749269 scopus 로고    scopus 로고
    • Congenital anomalies of the kidney and urinary tract-role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene
    • Pope JCT, Brock JW, Adams MC 3rd, Miyazaki Y, Stephens FD, Ichikawa I (2001) Congenital anomalies of the kidney and urinary tract-role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene. J Urol 165:196-202
    • (2001) J Urol , vol.165 , pp. 196-202
    • Pope, J.C.T.1    Brock, J.W.2    Adams III, M.C.3    Miyazaki, Y.4    Stephens, F.D.5    Ichikawa, I.6
  • 15
    • 0033860405 scopus 로고    scopus 로고
    • A molecular and genetic view of human renal and urinary tract malformations
    • Woolf AS (2000) A molecular and genetic view of human renal and urinary tract malformations. Kidney Int 58:500-512
    • (2000) Kidney Int , vol.58 , pp. 500-512
    • Woolf, A.S.1
  • 16
    • 0242660020 scopus 로고    scopus 로고
    • Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT
    • Miyazaki Y, Ichikawa I (2003) Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT. Pediatr Int 45:598-604
    • (2003) Pediatr Int , vol.45 , pp. 598-604
    • Miyazaki, Y.1    Ichikawa, I.2
  • 17
    • 0023477993 scopus 로고
    • Renal multicystic dysplasia: An occasional manifestation of the hereditary renal adysplasia syndrome
    • Squiers EC, Morden RS, Bernstein J (1987) Renal multicystic dysplasia: an occasional manifestation of the hereditary renal adysplasia syndrome. Am J Med Genet Suppl 3:279-284
    • (1987) Am J Med Genet , vol.3 , Issue.SUPPL. , pp. 279-284
    • Squiers, E.C.1    Morden, R.S.2    Bernstein, J.3
  • 18
    • 8344278949 scopus 로고    scopus 로고
    • ECLAMC: The Latin-American collaborative study of congenital malformations
    • Castilla EE, Orioli IM (2004) ECLAMC: the Latin-American collaborative study of congenital malformations. Community Genet 7:76-94
    • (2004) Community Genet , vol.7 , pp. 76-94
    • Castilla, E.E.1    Orioli, I.M.2
  • 19
    • 77953951780 scopus 로고    scopus 로고
    • The embryologic origin of ventral body wall defects
    • Sadler TW (2010) The embryologic origin of ventral body wall defects. Semin Pediatr Surg 19:209-214
    • (2010) Semin Pediatr Surg , vol.19 , pp. 209-214
    • Sadler, T.W.1
  • 25
    • 17444393534 scopus 로고    scopus 로고
    • Predictive factors of ultrasonographic involution of prenatally detected multicystic dysplastic kidney
    • Rabelo EA, Oliveira EA, Silva GS, Pezzuti IL, Tatsuo ES (2005) Predictive factors of ultrasonographic involution of prenatally detected multicystic dysplastic kidney. BJU Int 95:868-871
    • (2005) BJU Int , vol.95 , pp. 868-871
    • Rabelo, E.A.1    Oliveira, E.A.2    Silva, G.S.3    Pezzuti, I.L.4    Tatsuo, E.S.5
  • 26
    • 77950357285 scopus 로고    scopus 로고
    • Management in children of mild postnatal renal dilatation but without vesicoureteral reflux
    • Anderson NG, Fischer J, Leighton D, Hector-Taylor J, McEwing RL (2010) Management in children of mild postnatal renal dilatation but without vesicoureteral reflux. Pediatr Nephrol 25:477-483
    • (2010) Pediatr Nephrol , vol.25 , pp. 477-483
    • Anderson, N.G.1    Fischer, J.2    Leighton, D.3    Hector-Taylor, J.4    McEwing, R.L.5
  • 28
    • 42649136201 scopus 로고    scopus 로고
    • Antenatally detected urinary tract abnormalities: More detection but less action
    • Mallik M, Watson AR (2008) Antenatally detected urinary tract abnormalities: more detection but less action. Pediatr Nephrol 23:897-904
    • (2008) Pediatr Nephrol , vol.23 , pp. 897-904
    • Mallik, M.1    Watson, A.R.2
  • 29
    • 77956227829 scopus 로고    scopus 로고
    • Outcome and management of isolated severe renal pelvis dilatation detected at postnatal screening
    • Mami C, Palmara A, Paolata A, Marrone T, Marseglia L, Berte LF, Arena F (2010) Outcome and management of isolated severe renal pelvis dilatation detected at postnatal screening. Pediatr Nephrol 25:2093-2097
    • (2010) Pediatr Nephrol , vol.25 , pp. 2093-2097
    • Mami, C.1    Palmara, A.2    Paolata, A.3    Marrone, T.4    Marseglia, L.5    Berte, L.F.6    Arena, F.7
  • 30
    • 0242575908 scopus 로고    scopus 로고
    • Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT)
    • Nakanishi K, Yoshikawa N (2003) Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT). Pediatr Int 45:610-616
    • (2003) Pediatr Int , vol.45 , pp. 610-616
    • Nakanishi, K.1    Yoshikawa, N.2
  • 31
    • 0036919830 scopus 로고    scopus 로고
    • Malformations in newborn: Results based on 30, 940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998)
    • Queisser-Luft A, Stolz G, Wiesel A, Schlaefer K, Spranger J (2002) Malformations in newborn: results based on 30, 940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998). Arch Gynecol Obstet 266:163-167
    • (2002) Arch Gynecol Obstet , vol.266 , pp. 163-167
    • Queisser-Luft, A.1    Stolz, G.2    Wiesel, A.3    Schlaefer, K.4    Spranger, J.5
  • 32
    • 36849079873 scopus 로고    scopus 로고
    • Risk factors for urinary tract infection in children with prenatal renal pelvic dilatation
    • Coelho GM, Bouzada MC, Lemos GS, Pereira AK, Lima BP, Oliveira EA (2008) Risk factors for urinary tract infection in children with prenatal renal pelvic dilatation. J Urol 179:284-289
    • (2008) J Urol , vol.179 , pp. 284-289
    • Coelho, G.M.1    Bouzada, M.C.2    Lemos, G.S.3    Pereira, A.K.4    Lima, B.P.5    Oliveira, E.A.6
  • 34
    • 58249125438 scopus 로고    scopus 로고
    • Congenital hydronephrosis: Prenatal diagnosis and epidemiology in Europe
    • Garne E, Loane M, Wellesley D, Barisic I (2009) Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe. J Pediatr Urol 5:47-52
    • (2009) J Pediatr Urol , vol.5 , pp. 47-52
    • Garne, E.1    Loane, M.2    Wellesley, D.3    Barisic, I.4
  • 35
    • 21044444637 scopus 로고    scopus 로고
    • Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: An analysis of 709, 030 births in 12 European countries
    • Wiesel A, Queisser-Luft A, Clementi M, Bianca S, Stoll C (2005) Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709, 030 births in 12 European countries. Eur J Med Genet 48:131-144
    • (2005) Eur J Med Genet , vol.48 , pp. 131-144
    • Wiesel, A.1    Queisser-Luft, A.2    Clementi, M.3    Bianca, S.4    Stoll, C.5
  • 36
    • 0027448281 scopus 로고
    • Urological anomalies in the northern region fetal abnormality survey
    • Scott JE, Renwick M (1993) Urological anomalies in the Northern Region Fetal Abnormality Survey. Arch Dis Child 68:22-26
    • (1993) Arch Dis Child , vol.68 , pp. 22-26
    • Scott, J.E.1    Renwick, M.2
  • 38
    • 0036149194 scopus 로고    scopus 로고
    • Toward an etiological classification of developmental disorders of the kidney and upper urinary tract
    • Pohl M, Bhatnagar V, Mendoza SA, Nigam SK (2002) Toward an etiological classification of developmental disorders of the kidney and upper urinary tract. Kidney Int 61:10-19
    • (2002) Kidney Int , vol.61 , pp. 10-19
    • Pohl, M.1    Bhatnagar, V.2    Mendoza, S.A.3    Nigam, S.K.4
  • 39
    • 0036253480 scopus 로고    scopus 로고
    • Molecular mechanisms of human embryogenesis: Developmental pathogenesis of renal tract malformations
    • Woolf AS, Winyard PJ (2002) Molecular mechanisms of human embryogenesis: developmental pathogenesis of renal tract malformations. Pediatr Dev Pathol 5:108-129
    • (2002) Pediatr Dev Pathol , vol.5 , pp. 108-129
    • Woolf, A.S.1    Winyard, P.J.2
  • 41
  • 42
    • 0036318804 scopus 로고    scopus 로고
    • Fetal, perinatal, and infant death with congenital renal anomaly
    • Scott JE (2002) Fetal, perinatal, and infant death with congenital renal anomaly. Arch Dis Child 87:114-117
    • (2002) Arch Dis Child , vol.87 , pp. 114-117
    • Scott, J.E.1
  • 45
    • 78650119766 scopus 로고    scopus 로고
    • A retrospective cohort study of mortality among children with birth defects in New York State, 1983-2006
    • Wang Y, Hu J, Druschel CM (2010) A retrospective cohort study of mortality among children with birth defects in New York State, 1983-2006. Birth Defects Res A Clin Mol Teratol 88:1023-1031
    • (2010) Birth Defects Res A Clin Mol Teratol , vol.88 , pp. 1023-1031
    • Wang, Y.1    Hu, J.2    Druschel, C.M.3
  • 46
    • 32444445339 scopus 로고    scopus 로고
    • Determinants of survival in children with congenital abnormalities: A long-term population-based cohort study
    • Agha MM, Williams JI, Marrett L, To T, Dodds L (2006) Determinants of survival in children with congenital abnormalities: a long-term population-based cohort study. Birth Defects Res A Clin Mol Teratol 76:46-54
    • (2006) Birth Defects Res A Clin Mol Teratol , vol.76 , pp. 46-54
    • Agha, M.M.1    Williams, J.I.2    Marrett, L.3    To, T.4    Dodds, L.5
  • 47
    • 0037246479 scopus 로고    scopus 로고
    • Results of systematic screening for minor degrees of fetal renal pelvis dilatation in an unselected population
    • Ismaili K, Hall M, Donner C, Thomas D, Vermeylen D, Avni FE (2003) Results of systematic screening for minor degrees of fetal renal pelvis dilatation in an unselected population. Am J Obstet Gynecol 188:242-246
    • (2003) Am J Obstet Gynecol , vol.188 , pp. 242-246
    • Ismaili, K.1    Hall, M.2    Donner, C.3    Thomas, D.4    Vermeylen, D.5    Avni, F.E.6
  • 48
    • 21844459526 scopus 로고    scopus 로고
    • Insights into the pathogenesis and natural history of fetuses with renal pelvis dilatation
    • Ismaili K, Hall M, Piepsz A, Alexander M, Schulman C, Avni FE (2005) Insights into the pathogenesis and natural history of fetuses with renal pelvis dilatation. Eur Urol 48:207-214
    • (2005) Eur Urol , vol.48 , pp. 207-214
    • Ismaili, K.1    Hall, M.2    Piepsz, A.3    Alexander, M.4    Schulman, C.5    Avni, F.E.6
  • 49
    • 77953501749 scopus 로고    scopus 로고
    • Prenatal management of urogenital disorders
    • Carr MC, Kim SS (2010) Prenatal management of urogenital disorders. Urol Clin North Am 37:149-158
    • (2010) Urol Clin North Am , vol.37 , pp. 149-158
    • Carr, M.C.1    Kim, S.S.2


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