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Volumn 23, Issue 4, 2004, Pages 211-229

Developmental renal pathology: Its past, present, and future

Author keywords

Diabetic embryopathy; Pharmacogenetics; Polycystic kidneys; Post natal renal development; Renal agenesis; Renal dysplasia

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CONGENITAL DISORDER; DIAGNOSTIC TEST; ECHOGRAPHY; EMBRYOLOGY; EMBRYOPATHY; HUMAN; HYDRONEPHROSIS; KIDNEY AGENESIS; KIDNEY DEVELOPMENT; KIDNEY DYSPLASIA; KIDNEY FUNCTION; KIDNEY INJURY; KIDNEY POLYCYSTIC DISEASE; MOLECULAR BIOLOGY; OLIGOHYDRAMNIOS; PERINATAL PERIOD; PHARMACOGENETICS; PRIORITY JOURNAL; REVIEW; VESICOURETERAL REFLUX; CHILD; FETUS; KIDNEY; KIDNEY DISEASE; PATHOLOGY; PRENATAL DEVELOPMENT; URINARY TRACT; URINARY TRACT DISEASE;

EID: 24044470028     PISSN: 15513815     EISSN: 15513823     Source Type: Journal    
DOI: 10.1080/15227950490923453     Document Type: Review
Times cited : (17)

References (61)
  • 1
    • 0041630593 scopus 로고    scopus 로고
    • Chronic renal insufficiency in children: The 2001 annual report of the NAPRTCS
    • Seikaly MG, Ho PL, Emmett L, Fine RN, Tejani A. Chronic renal insufficiency in children: the 2001 annual report of the NAPRTCS. Pediatr Nephrol 2003;18:796-804.
    • (2003) Pediatr Nephrol , vol.18 , pp. 796-804
    • Seikaly, M.G.1    Ho, P.L.2    Emmett, L.3    Fine, R.N.4    Tejani, A.5
  • 2
    • 0033781313 scopus 로고    scopus 로고
    • The EPICure study: Outcomes to discharge from hospital for infants born at the threshold of viability
    • Costeloe K, Hennessy E, Gibson AT, Marlow N, Wilkinson AR. The EPICure study: outcomes to discharge from hospital for infants born at the threshold of viability. Pediatrics 2000;106:659-671.
    • (2000) Pediatrics , vol.106 , pp. 659-671
    • Costeloe, K.1    Hennessy, E.2    Gibson, A.T.3    Marlow, N.4    Wilkinson, A.R.5
  • 3
    • 0029036339 scopus 로고
    • Effects of ureteral obstruction on renal growth
    • Chevalier RL. Effects of ureteral obstruction on renal growth. Semin Nephrol 1995;15:353-360.
    • (1995) Semin Nephrol , vol.15 , pp. 353-360
    • Chevalier, R.L.1
  • 4
    • 0001934046 scopus 로고
    • Urogenital system
    • Baltimore: Williams & Wilkins
    • Sadler TW. Urogenital system. In eds. Langman's Medical Embryology. Baltimore: Williams & Wilkins, 1990, p.260.
    • (1990) Langman's Medical Embryology , pp. 260
    • Sadler, T.W.1
  • 6
    • 0028307612 scopus 로고
    • Pharmacology of antineoplastic agents in pregnancy
    • Wiebe VJ, Sipila PE. Pharmacology of antineoplastic agents in pregnancy. Crit Rev Oncol Hematol 1994;16:75-112.
    • (1994) Crit Rev Oncol Hematol , vol.16 , pp. 75-112
    • Wiebe, V.J.1    Sipila, P.E.2
  • 7
    • 84872623412 scopus 로고
    • Facial characteristics of infants with bilateral renal agenesis
    • Potter EL. Facial characteristics of infants with bilateral renal agenesis. Am J Obstet Gynecol 1946;41:885-888.
    • (1946) Am J Obstet Gynecol , vol.41 , pp. 885-888
    • Potter, E.L.1
  • 9
    • 0029590072 scopus 로고
    • Pax-2 controls multiple steps of urogenital development
    • Torres M, Gomez-Pardo E, Dressler Gr, Gruss P. Pax-2 controls multiple steps of urogenital development. Development 1995;121:4057-4065.
    • (1995) Development , vol.121 , pp. 4057-4065
    • Torres, M.1    Gomez-Pardo, E.2    Dressler, Gr.3    Gruss, P.4
  • 11
    • 0019362340 scopus 로고
    • The pathogenesis of renal dysplasia II. The significance of lateral and medial ectopy of the ureteric orifice
    • Schwarz RD, Stephens FD, Gussen LJ. The pathogenesis of renal dysplasia II. The significance of lateral and medial ectopy of the ureteric orifice. Invest Urol 1981;19:97-100.
    • (1981) Invest Urol , vol.19 , pp. 97-100
    • Schwarz, R.D.1    Stephens, F.D.2    Gussen, L.J.3
  • 12
    • 0015609511 scopus 로고
    • Position and configuration of the ureteral orifice and its relationship to renal scarring in adults
    • Vermillion CD, Heale WF. Position and configuration of the ureteral orifice and its relationship to renal scarring in adults. J Urol 1973;109:579-584.
    • (1973) J Urol , vol.109 , pp. 579-584
    • Vermillion, C.D.1    Heale, W.F.2
  • 13
  • 14
    • 0027756731 scopus 로고
    • A quantitative study of normal nephrogenesis in the human fetus: Its implications in the natural history of kidney changes due to low obstructive uropathies
    • Gasser B, Mauss Y, Ghnassia JP, Kohler M, Yu O, Vonesch JL. A quantitative study of normal nephrogenesis in the human fetus: its implications in the natural history of kidney changes due to low obstructive uropathies. Fetal Diagn Ther 1993;8:371-384.
    • (1993) Fetal Diagn Ther , vol.8 , pp. 371-384
    • Gasser, B.1    Mauss, Y.2    Ghnassia, J.P.3    Kohler, M.4    Yu, O.5    Vonesch, J.L.6
  • 16
    • 0043131813 scopus 로고    scopus 로고
    • Prenatal ultrasound guided percutaneous shunts for obstructive uropathy and thoracic disease
    • Wilson RD, Johnson MP. Prenatal ultrasound guided percutaneous shunts for obstructive uropathy and thoracic disease. Semin Pediatr Surg 2003;12:182-189.
    • (2003) Semin Pediatr Surg , vol.12 , pp. 182-189
    • Wilson, R.D.1    Johnson, M.P.2
  • 19
    • 0021339670 scopus 로고
    • Familial nature of congenital absence and severe dysgenesis of both kidneys
    • Roodhoof AM, Birnholtz JC, Holmes LB. Familial nature of congenital absence and severe dysgenesis of both kidneys. N Engl J Med 1984;310:1341-1345.
    • (1984) N Engl J Med , vol.310 , pp. 1341-1345
    • Roodhoof, A.M.1    Birnholtz, J.C.2    Holmes, L.B.3
  • 20
    • 12644280361 scopus 로고
    • Unilateral hereditary hydronephrosis: A report of four cases in three consecutive generations
    • Jewell JH, Buchert WI. Unilateral hereditary hydronephrosis: a report of four cases in three consecutive generations. J Urol 1962;88:129-136.
    • (1962) J Urol , vol.88 , pp. 129-136
    • Jewell, J.H.1    Buchert, W.I.2
  • 21
    • 0026744209 scopus 로고
    • Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p
    • Izquierdo L, Porteous M, Paramo PG, Conner JM. Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6p. Hum Genet 1992;89:557-560.
    • (1992) Hum Genet , vol.89 , pp. 557-560
    • Izquierdo, L.1    Porteous, M.2    Paramo, P.G.3    Conner, J.M.4
  • 22
    • 0030447827 scopus 로고    scopus 로고
    • Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia
    • Groener PM, Garcia E, Debeer P, Devriendt K, Fryns JP, Van de Ven WJ. Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia. Genomics 1996;38:141-148.
    • (1996) Genomics , vol.38 , pp. 141-148
    • Groener, P.M.1    Garcia, E.2    Debeer, P.3    Devriendt, K.4    Fryns, J.P.5    Van De Ven, W.J.6
  • 23
    • 0026455194 scopus 로고
    • The transmission of vesico-ureteral reflux from parent to child
    • Noe HN, Wyatt RJ, Peeden JN, Rivas ML. The transmission of vesico-ureteral reflux from parent to child. J Urol 1992;148:1869-1871.
    • (1992) J Urol , vol.148 , pp. 1869-1871
    • Noe, H.N.1    Wyatt, R.J.2    Peeden, J.N.3    Rivas, M.L.4
  • 24
    • 0036837263 scopus 로고    scopus 로고
    • Screening siblings for vesico-ureteral reflux
    • Hollowell JG, Greenfield SP. Screening siblings for vesico-ureteral reflux. J Urol 2002;168:2138-2141.
    • (2002) J Urol , vol.168 , pp. 2138-2141
    • Hollowell, J.G.1    Greenfield, S.P.2
  • 25
    • 0033910650 scopus 로고    scopus 로고
    • Primary nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1
    • Feather SA, Malcolm S, Woolf AS, Wright V, Blaydon D, Reid CJ, et al. Primary nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1. Am J Hum Genet 2000;66:1420-1425.
    • (2000) Am J Hum Genet , vol.66 , pp. 1420-1425
    • Feather, S.A.1    Malcolm, S.2    Woolf, A.S.3    Wright, V.4    Blaydon, D.5    Reid, C.J.6
  • 26
    • 0021280772 scopus 로고
    • The Meckel syndrome: Clinicopathological findings in 67 patients
    • Salonen R. The Meckel syndrome: clinicopathological findings in 67 patients. Am J Med Genet 1984;18:671-689.
    • (1984) Am J Med Genet , vol.18 , pp. 671-689
    • Salonen, R.1
  • 29
    • 0033615563 scopus 로고    scopus 로고
    • Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome
    • Fujimoto S, Yokochi K, Morikawa H, Nakano M, Shibata H, Togari H, Wada Y. Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome. Am J Med Genet 1999;86:427-429.
    • (1999) Am J Med Genet , vol.86 , pp. 427-429
    • Fujimoto, S.1    Yokochi, K.2    Morikawa, H.3    Nakano, M.4    Shibata, H.5    Togari, H.6    Wada, Y.7
  • 30
    • 0026728345 scopus 로고
    • Brief report: Autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia
    • Bilous RW, Murty G, Parkinson DB, Thakker RV, Coulthard MG, Burn J, et al. Brief report: autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia. N Engl J Med 1992;327:1069-1074.
    • (1992) N Engl J Med , vol.327 , pp. 1069-1074
    • Bilous, R.W.1    Murty, G.2    Parkinson, D.B.3    Thakker, R.V.4    Coulthard, M.G.5    Burn, J.6
  • 35
    • 0021347101 scopus 로고
    • New syndrome: Renal dysplasia, mesomelia, and radiohumeral fusion
    • Ulbright CE, Hodes ME, Ulbright TM. New syndrome: renal dysplasia, mesomelia, and radiohumeral fusion. Am J Med Genet 1984;17:667-668.
    • (1984) Am J Med Genet , vol.17 , pp. 667-668
    • Ulbright, C.E.1    Hodes, M.E.2    Ulbright, T.M.3
  • 36
    • 0025025724 scopus 로고
    • Limb reduction defects and renal dysplasia: Confirmation of a new, apparently lethal, autosomal recessive MCA syndrome
    • Schrander-Stumpel C, de Die-Smulders C, Fryns JP, da Costa J, Bouckaert P. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome. Am J Med Genet 1990;37:133-135.
    • (1990) Am J Med Genet , vol.37 , pp. 133-135
    • Schrander-Stumpel, C.1    De Die-Smulders, C.2    Fryns, J.P.3    Da Costa, J.4    Bouckaert, P.5
  • 38
    • 0032513573 scopus 로고    scopus 로고
    • Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13
    • Kumar S, Marres HA, Cor WR, Cremers CW, Kimberling WJ. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13. Am J Med Genet 1998;76:395-401.
    • (1998) Am J Med Genet , vol.76 , pp. 395-401
    • Kumar, S.1    Marres, H.A.2    Cor, W.R.3    Cremers, C.W.4    Kimberling, W.J.5
  • 39
    • 0033942027 scopus 로고    scopus 로고
    • Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: Clinical and genetic implications
    • Kumar S, Deffenbacher K, Marres HA, Cor WR, Cremers CW, Kimberling WJ. Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications. Am J Hum Genet 2000;66:1715-1720.
    • (2000) Am J Hum Genet , vol.66 , pp. 1715-1720
    • Kumar, S.1    Deffenbacher, K.2    Marres, H.A.3    Cor, W.R.4    Cremers, C.W.5    Kimberling, W.J.6
  • 41
    • 0035180570 scopus 로고    scopus 로고
    • Embryonic gut anomalies in a mouse model of retinoic acid-induced caudal regression syndrome
    • Pitera JE, Smith VV, Wolf AS, Milla PJ. Embryonic gut anomalies in a mouse model of retinoic acid-induced caudal regression syndrome. Am J Pathol 2001;159:2321-2329.
    • (2001) Am J Pathol , vol.159 , pp. 2321-2329
    • Pitera, J.E.1    Smith, V.V.2    Wolf, A.S.3    Milla, P.J.4
  • 43
    • 0346335999 scopus 로고    scopus 로고
    • Renal development in high-glucose ambience and diabetic embryopathy
    • Chugh SS, Wallner EI, Kanwar YS. Renal development in high-glucose ambience and diabetic embryopathy. Semin Nephrol 2003;23:583-592.
    • (2003) Semin Nephrol , vol.23 , pp. 583-592
    • Chugh, S.S.1    Wallner, E.I.2    Kanwar, Y.S.3
  • 44
    • 0024592194 scopus 로고
    • Evidence of multifactorial origin of diabetes-induced embryopathies
    • Sadler TW, Hunter ES, Wynn RE, Phillips LS. Evidence of multifactorial origin of diabetes-induced embryopathies. Diabetes 1989;38:70-74.
    • (1989) Diabetes , vol.38 , pp. 70-74
    • Sadler, T.W.1    Hunter, E.S.2    Wynn, R.E.3    Phillips, L.S.4
  • 45
    • 0033857531 scopus 로고    scopus 로고
    • The missing link: A single unifying mechanism for diabetic complications
    • Nishikawa T, Edelstein D, Brownlee M. The missing link: a single unifying mechanism for diabetic complications. Kidney Int Suppl 2000;77:S26-S30.
    • (2000) Kidney Int Suppl , vol.77
    • Nishikawa, T.1    Edelstein, D.2    Brownlee, M.3
  • 46
    • 0036724696 scopus 로고    scopus 로고
    • Diacylglycerol production and protein kinase C activity are increased in a mouse model of diabetic embryopathy
    • Hiramatsu Y, Sekiguchi N, Hayashi M, Issihiki K, Yokota T, King GL, Loeken MR. Diacylglycerol production and protein kinase C activity are increased in a mouse model of diabetic embryopathy. Diabetes 2002;51:2804-2810.
    • (2002) Diabetes , vol.51 , pp. 2804-2810
    • Hiramatsu, Y.1    Sekiguchi, N.2    Hayashi, M.3    Issihiki, K.4    Yokota, T.5    King, G.L.6    Loeken, M.R.7
  • 47
    • 0023940456 scopus 로고
    • Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family
    • Kaplan BS, Kaplan P, de Chadarevian JP, Jequier S, O'Regan S, Russo P. Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family. Am J Med Genet 1988;29:639-647.
    • (1988) Am J Med Genet , vol.29 , pp. 639-647
    • Kaplan, B.S.1    Kaplan, P.2    De Chadarevian, J.P.3    Jequier, S.4    O'Regan, S.5    Russo, P.6
  • 48
    • 0036509712 scopus 로고    scopus 로고
    • The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
    • Ward CJ, Hogan MC, Rossetti S, Walker D, Sneddon T, Wang X, et al. The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein. Nat Genet 2002;30:259-269.
    • (2002) Nat Genet , vol.30 , pp. 259-269
    • Ward, C.J.1    Hogan, M.C.2    Rossetti, S.3    Walker, D.4    Sneddon, T.5    Wang, X.6
  • 49
    • 0345304730 scopus 로고    scopus 로고
    • Molecular genetics of autosomal dominant polycystic kidney disease
    • Pei Y. Molecular genetics of autosomal dominant polycystic kidney disease. Clin Invest Med, 2003;26:252-258.
    • (2003) Clin Invest Med , vol.26 , pp. 252-258
    • Pei, Y.1
  • 51
    • 0028030817 scopus 로고
    • Incidence of renal anomalies in children prenatally exposed to ethanol
    • Taylor CL, Jones KL, Jones MC, Kaplan GW. Incidence of renal anomalies in children prenatally exposed to ethanol. Pediatrics 1994;94:209-212.
    • (1994) Pediatrics , vol.94 , pp. 209-212
    • Taylor, C.L.1    Jones, K.L.2    Jones, M.C.3    Kaplan, G.W.4
  • 52
    • 0025875281 scopus 로고
    • Pathogenesis of ethanol-induced hydronephrosis and hydroureter as demonstrated following in vivo exposure of mouse embryos
    • Gage JC, Sulick KK. Pathogenesis of ethanol-induced hydronephrosis and hydroureter as demonstrated following in vivo exposure of mouse embryos. Teratology 1991;44:299-312.
    • (1991) Teratology , vol.44 , pp. 299-312
    • Gage, J.C.1    Sulick, K.K.2
  • 53
    • 0035862977 scopus 로고    scopus 로고
    • The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures
    • Abu-Abed S, Dolle P, Metzger D, Beckett B, Chambon P, Petkovich M. The retinoic acid-metabolizing enzyme, CYP26A1, is essential for normal hindbrain patterning, vertebral identity, and development of posterior structures. Genes Dev 2001;15:226-240.
    • (2001) Genes Dev , vol.15 , pp. 226-240
    • Abu-Abed, S.1    Dolle, P.2    Metzger, D.3    Beckett, B.4    Chambon, P.5    Petkovich, M.6
  • 55
    • 0042030805 scopus 로고    scopus 로고
    • Investigating the newborn kidney: Update on imagin technique
    • Gordon I, Riccabona M. Investigating the newborn kidney: update on imagin technique. Semin Neonatol 2003;8:269-278.
    • (2003) Semin Neonatol , vol.8 , pp. 269-278
    • Gordon, I.1    Riccabona, M.2
  • 56
    • 8344272186 scopus 로고    scopus 로고
    • Is there significant improvement in neonatal outcome after treating pPROM mothers with ammo-infusion?
    • De Carolis MP, Romagnoli C, de Santis M, Piersigilli F, Vento G, Caruso A. Is there significant improvement in neonatal outcome after treating pPROM mothers with ammo-infusion? Biol Neonate 2004;8:222-229.
    • (2004) Biol Neonate , vol.8 , pp. 222-229
    • De Carolis, M.P.1    Romagnoli, C.2    De Santis, M.3    Piersigilli, F.4    Vento, G.5    Caruso, A.6
  • 57
    • 0042697656 scopus 로고    scopus 로고
    • Prenatal bladder drainage in the management of fetal lower urinary tract obstruction: A systematic review and meta-analysis
    • Clark TJ, Martin WL, Divakaran TG, Whittle MJ, Kilby MD, Khan KS. Prenatal bladder drainage in the management of fetal lower urinary tract obstruction: a systematic review and meta-analysis. Obstet Gynecol 2003;102:367-382.
    • (2003) Obstet Gynecol , vol.102 , pp. 367-382
    • Clark, T.J.1    Martin, W.L.2    Divakaran, T.G.3    Whittle, M.J.4    Kilby, M.D.5    Khan, K.S.6
  • 61
    • 0030733083 scopus 로고    scopus 로고
    • Glial-cell-line derived neurotrophic factor is required for bud initiation from ureteric epithelium
    • Saino K, Suvanto P, Davies J, Wartiovaara J, Wartiovaara K, Saarma M, et al. Glial-cell-line derived neurotrophic factor is required for bud initiation from ureteric epithelium. Development 1997;124:407-487.
    • (1997) Development , vol.124 , pp. 407-487
    • Saino, K.1    Suvanto, P.2    Davies, J.3    Wartiovaara, J.4    Wartiovaara, K.5    Saarma, M.6


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