Skip to main content

Krankheiten der Niere, der ableitenden Harnwege und des äußeren Genitales

  • Chapter
Pädiatrie

Zusammenfassung

Die Aufgabe der Niere ist die Aufrechterhaltung der Homöostase sowie des Salz-Wasser- und des Säure-Basen-Haushaltes. Intrauterin hat die Urinproduktion wesentlichen Anteil an der Fruchtwassermenge. Bei intrauterin fehlender Urinproduktion kommt es zu sekundären Folgen durch mechanische Kompression des Fetus mit Mißbildungssyndromen. Die glomeruläre Filtrationsrate ist intrauterin einem langsamen Entwicklungsprozeß unterworfen. Bei Frühgeburten ab der 23. Schwangerschaftswoche ist eine ausreichende glomeruläre Filtration vorhanden. Die relative Expansion des Extrazellulärvolumens bei Frühgeborenen führt postnatal innerhalb weniger Tage zu einer erhöhten Ausscheidung von Flüssigkeit und NaCl. Dieser hohe Salzverlust in den ersten Lebenstagen ist nicht Ausdruck einer renal-tubulären Unreife, sondern Folge der Reduktion des Extrazellulärvolumens. Als Ausdruck dieser erhöhten NaCl-Exkretion ist die fraktionelle Natriumausscheidung bei Frühgeborenen deutlich höher als bei Reifgeborenen (1–7% vs. 1%). Die Adaptation des Flüssigkeitshaushaltes führt bei Neugeborenen innerhalb der ersten Lebenstage zu einem physiologischen Gewichtsverlust von bis zu 10% des Ausgangsgeburtsgewichtes. Die Balance zwischen Salz- und Wasserzufuhr und Neigung zur Reduktion des Extrazellulärvolumens ist Voraussetzung für die Konstanz der Natriumkonzentration im Plasma. Infolge einer nicht adäquaten Substitution an Wasser und Salz kann bei Frühgeborenen eine Hyponatriämie entstehen. Die Regulation des Säure-Basen-Haushaltes wird beeinflußt durch einen relativ hohen Bicarbonatverlust durch den proximalen Tubulus bei Frühgeborenen. Dieser ist bevorzugt bedingt durch eine relative Expansion des Extrazellulärvolumens. Die Sekretionsfähigkeit für H-Ionen ist auch bei einer Frühgeborenenniere schon voll vorhanden. Es besteht keine relative Unreife der Frühgeborenenniere bei der Regulation des Säure-Basen-Haushaltes. Intrauterin besteht keine Notwendigkeit, den Harn zu konzentrieren. Nach der Geburt entwickelt sich erst langsam die Fähigkeit, die Urinkonzentration über 350 mosmol/1 anzuheben. Dies ist partiell bedingt durch eine hohe Prostaglandinsekretion, die die Kochsalzresorption hemmt und die Permeabilität für Harnstoff entlang des Tubulus inhibiert. Innerhalb weniger Tage bis Wochen ändert sich dieser Zustand, und die Konzentrierungsfähigkeit steigt bis auf 600–800 mosmol/1 an.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 54.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literatur

  • Arant B (1991) Vesicoureteric reflux and renal injury. Am J Kidney Dis 17: 491

    PubMed  Google Scholar 

  • Bailey RR, Rolleston GL (1997) Vesicoureteric reflux and reflux nephropathy: the Christchurch contribution. N Z Med J no: 266–269

    Google Scholar 

  • Caione P, Patricolo M, Lais A, Capitanucci ML, Capozza N, Ferro F (1996) Role of prenatal diagnosis in the treatment of congenital obstructive megaureter. Fetal Diagn Ther 11, 205–209

    Article  PubMed  CAS  Google Scholar 

  • Docimo SG, Silver RI (1997) Renal ultrasonography in newborns with prenatally detected hydronephrosis: why wait? J Uro1157: 1387–1389

    Google Scholar 

  • Elder JS (1997) Antenatal hydronephrosis. Fetal and neonatal management. Pediatr Clin North Am 44: 1299–1321

    Article  PubMed  CAS  Google Scholar 

  • Hawkins EP (1994) Morphologic development of the kidney. In: Oski FA (ed) Principles and practice of paediatrics, 2nd edn. Lippincott, Philadelphia, pp 1752–1753

    Google Scholar 

  • Reinberg Y, Castano I de, Gonzalez R (1992) Prognosis for patients with prenatally diagnosed posterior urethral valves. J Urol 148: 125–126

    PubMed  CAS  Google Scholar 

  • Scott JE, Swallow V, Coulthard MG, Lambert HJ, Lee RE (1997) Screening of newborn babies for familial ureteric reflux. Lancet 350: 396–400

    Article  PubMed  CAS  Google Scholar 

  • Stormann J, Kuwertz-Broking E, Hentschel R et al. (1995) Interdisciplinary management of fetal obstructive uropathy. Z Geburtshilfe Neonato1199: 257–261

    Google Scholar 

  • Yu TJ, Chen WF (1997) Surgical management of grades III and IV primary vesicoureteral reflux in children with and without acute pyelonephritis as breakthrough infections: a comparative analysis. J Urol 157: 1404–1406

    Article  PubMed  CAS  Google Scholar 

  • Blyth H, Ockenden BG (1971) Polycystic disease of kidneys and liver presenting in childhood. J Med Genet 8: 257

    Article  PubMed  CAS  Google Scholar 

  • Brook-Carter PT, Peral B, Ward CJ et al. (1994) Deletion of the TSC2 and PKDi genes associated with severe infantile polycystic kidney disease–a contigous gene syndrome. Nat Genet 8: 328–332

    Article  PubMed  CAS  Google Scholar 

  • Green JS, Parfrey PS, Harnett JD et al. (1989) The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome. N Engl J Med 321: 1002–1009

    Article  PubMed  CAS  Google Scholar 

  • Kern S, Zimmerhackl LB, Hildebrandt F, Ermisch-Omran B, Uhl M (2000) Appearance of autosomal recessive polycystic kidney disease in magnetic resonance imaging and RARE-MR-urography. Pediatr Radio! 30: 156–160

    Article  CAS  Google Scholar 

  • Potter EL (1965) Bilateral absence of ureters and kidneys: a report of 5o cases. Obstet Gynecol 25: 3

    PubMed  CAS  Google Scholar 

  • Sampson JR, Maheshwar MM, Aspinwall R et al. (1997) Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene. Am J Hum Genet 61: 843–851

    Article  PubMed  CAS  Google Scholar 

  • Zerres K (1992) Autosomal recessive polycystic kidney disease. Clin Invest 70: 794–801

    Article  CAS  Google Scholar 

  • Zerres K, Rudnik-Schöneborn S, Steinkamm C, Becker J, Mücher G (1998) Autosomal recessive polycystic kidney disease. J Mol Med 76: 303–309

    Article  PubMed  CAS  Google Scholar 

  • Brook-Carter PT, Peral B, Ward CJ et al. (1994) Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease–a contigous gene syndrome. Nat Genet 8: 328–332

    Article  PubMed  CAS  Google Scholar 

  • Mc Donald RA, Watkins LS, Avner ED (1999) Polycystic kidney disease. In: Barratt TM, Avner ED, Harmon WE (eds) Pediatric nephrology, 4th edn. Lippincott, Williams & Witkins, Baltimore, pp 459–474

    Google Scholar 

  • Sampson JR, Maheshwar MM, Aspinwall R et al. (1997) Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene. Am J Hum Genet 61: 843–851

    Article  PubMed  CAS  Google Scholar 

  • Boichis H, Passwell J, David R et al. (1973) Congenital hepatic fibrosis and nephronophthisis. OJM 42: 221–233

    CAS  Google Scholar 

  • Fuchshuber A, Deltas CC, Berthold S et al. (1998) Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneity. Nephrol Dial Transplant 13: 1955–1957

    Article  PubMed  CAS  Google Scholar 

  • Gardner KD Jr, Evan AP (1979) Nephronophthisis and medullary cystic disease. In: Hamburger J, Crosnier J, Grünfeld J-P (eds) Nephrology. Wiley, New York, pp 922–935

    Google Scholar 

  • Hildebrandt F, Jungers P, Grünfeld J-P (1996) Medullary cystic and medullary sponge renal disorders. In: Schrier WB, Gottschalk C (eds) Diseases of the kidney. Little Brown, Boston, pp 499–520

    Google Scholar 

  • Hildebrandt F, Otto E, Rensing C et al. (1997a) A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1. Nat Genet 17: 149–153

    Article  PubMed  CAS  Google Scholar 

  • Hildebrandt F, Strahm B, Nothwang HG et al. (1997b) Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie. Kidney Int 51: 261–269

    Google Scholar 

  • Hildebrandt F (1999) Juvenile Nephronophthisis. In: Avner ED, Holliday MA, Barratt TM (eds) Pediatric nephrology. Lippincott, Williams & Wilkins, Baltimore, pp 453–458

    Google Scholar 

  • Leken AC, Haussen O, Halvorsen S, Jelster NJ (1961) Hereditary renal dysplasia and blindness. Acta Paediatr 5o: 177–184

    Article  Google Scholar 

  • Moudgil A, Bagga A, Kamil ES et al. (1998) Nephronophthisis associated with Ellis-van Creveld syndrome. Pediatr Nephrol 12: 20–22

    Article  PubMed  CAS  Google Scholar 

  • Nothwang HG, Stubanus M, Adolphs J et al. (1998) Construction of a gene map of the nephronophthisis type s(NPHP1) region on human chromosome 2g12-q13. Genomics 47: 276–285

    Article  PubMed  CAS  Google Scholar 

  • Senior B, Friedmann AI, Braudo JL (1961) Juvenile familial nephropathy with tapetoretinal degeneration: a new oculorenal dystrophy. Am J Ophthalmol 52: 625–633

    PubMed  CAS  Google Scholar 

  • Waldherr R, Lennert T, Weber HP, Födisch HJ, Schärer K (1982) The nephronophthisis complex: a clinicopathologic study in children. Virchows Arch A 394: 235–254

    CAS  Google Scholar 

  • Hildebrandt F, Jungers P, Grünfeld J-P (1996) Medullary cystic and medullary sponge renal disorders. In: Schrier WB, Gottschalk C (eds) Diseases of the kidney. Little Brown, Boston, pp 499–520

    Google Scholar 

  • Jeune M, Beraud C, Carron R (1955) Dystrophie thoracique asphyxiante de caractere familial. Arch Franc Pediatr 12: 886–891

    Google Scholar 

  • Opitz JM, Howe JJ (1969) The Meckel syndrome (dysencephalia splanchnocystica, the Gruber syndrome). Birth Defects Orig Art Ser V (2): 167–179

    Google Scholar 

  • Watkins SL, Mc Donald RA, Avner ED (1999) Renal dysplasia, hypoplasia, and miscellaneous cystic disorder. In: Barratt TM, Avner ED, Harmon WE (eds) Pediatric nephrology. Lippincott, Williams & Wilkins, Baltimore, pp 415–426

    Google Scholar 

  • Zerres K (1992) Autosomal recessive polycystic kidney disease. Clin Invest 70: 794–801

    Article  CAS  Google Scholar 

  • Clark AG, Barratt TM (1999) Steroid responsive nephrotic syndrome. In: Barratt FM, Avner ED, Harmon WE (eds) Pediatric nephrology. Lippincott, Williams & Wilkins, Baltimore, pp 731–747

    Google Scholar 

  • Donckerwolcke RA, Vande Walle JG (1997) Pathogenesis of edema for- mation in the nephrotic syndrome. Kidney Int Suppl 58: 72–74

    Google Scholar 

  • Fuchshuber A, Niaudet P, Gribouval O, Jean G, Gubler MC, Broyer M, Antignac C (1996) Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population. Pediatr Nephrol 10: 135–138

    PubMed  CAS  Google Scholar 

  • Hisano S, Hahn S, Kuemmerle NB, Chan JC, DeSanto NG (1997) Edema in childhood. Kidney Int Suppl 59: 100–104

    Google Scholar 

  • Holmberg C, Laine J, Ronnholm K, Ala-Houhala M, Jalanko H (1996) Congenital nephrotic syndrome. Kidney Int Supp153: 51–56

    Google Scholar 

  • Mendoza SA, Tune BM (1995) Management of the difficult nephrotic patient. Pediatr Clin North Am 42: 1459–1468

    PubMed  CAS  Google Scholar 

  • Milford DV (1995) The nephrotic syndrome. Br J Hosp Med 53: 147–151

    PubMed  CAS  Google Scholar 

  • Orth SR, Ritz E (1998) The nephrotic syndrome. N Engl J Med 338: 1202–1211

    Article  PubMed  CAS  Google Scholar 

  • Schnaper HW (1996) Primary nephrotic syndrome of childhood. Curr Opin Pediatr 8: 141–147

    Article  PubMed  CAS  Google Scholar 

  • Andreoli SP (1998) Renal manifestations of systemic diseases. Semin Nephrol 18: 270–279

    PubMed  CAS  Google Scholar 

  • Baqi N, Moazami S, Singh A, Ahmad H, Balachandra S, Tejani A (1996) Lupus nephritis in children: a longitudinal study of prognostic factors and therapy. J Am Soc Nephrol 7: 924–929

    Google Scholar 

  • Clark GWR, Glasgow EF, Chantler C et al. (1988) Poststreptococcal glomerulonephritis in children: clinicopathologic correlation and longterm prognosis. Pediatr Nephrol 2: 381

    Article  PubMed  CAS  Google Scholar 

  • Higgins PM (1996) Acute poststreptococcal glomerulonephritis in general practice: the contribution of infection to its onset and course. Epidemiol Infect 116: 193–201

    Article  PubMed  CAS  Google Scholar 

  • Mosca M, Pasquariello A, Tavoni A et al. (1997) Predictors of renal outcome in diffuse proliferative glomerulonephritis in systemic lupus erythematosus. Lupus 6: 371–378

    Article  PubMed  CAS  Google Scholar 

  • Philipp LB, Brewer E (1994) Glomerulonephritis and nephrotic syndrome. In: Oski FA (ed) Principles and practice of pediatrics, 2nd edn. Lippincott, Philadelphia, pp 1785–1802

    Google Scholar 

  • Wyatt RJ, Kritchevsky SB, Woodford SY et al. (1995) IgA nephropathy: long-term prognosis for pediatric patients. J Pediatr 127: 913–919

    Google Scholar 

  • Andrioli SP (1998) Management of acute renal failure. Barratt TM,Avner ED, Harmon WE (eds) Pediatric Nephrology. Lippincott, Williams & Witkins, pp 1119–1134

    Google Scholar 

  • Bitzan M, Moebius E, Ludwig K, Müller-Wiefel DE, Heesemann J, Karch H (1991) High incidence of serum antibodies to Escherichia coli O157 lipopolysaccharide in children with hemolytic uremic syndrome. J Pediatr 119: 380–385

    Article  PubMed  CAS  Google Scholar 

  • Gasser C, Gautier E, Steck A, Siebenmann RE, Oechslin R (1955) Hämolytisch-urämische Syndrome: Bilaterale Nierenrindennekrosen bei akuten erworbenen Anämien. Schweiz Med Wochenschr 85: 905–909

    Google Scholar 

  • Kar NCAJ van der, Hinsbergh VWM van, Brommer EJP, Monnens LAH (1994) The fibrinolytic system in hemolytic uremic syndrome: in vivo and in vitro studies. Pediatr Res 36: 257–264

    Google Scholar 

  • Karch H (1996) Control of enterohemorrhagic Escherichia coli infection–the need for a network involving microbiological laboratories and clinical and public health institutions. Eur J Clin Microbiol Infect Dis 15: 276–280

    Article  PubMed  CAS  Google Scholar 

  • Repetto HA (1997) Epidemic hemolytic-uremic syndrome in children. Kidney Int 52: 1708–1719

    Article  PubMed  CAS  Google Scholar 

  • Siegler R (1995) The hemolytic uremic syndrome. Pediatr Clin North Am 42: 1039–1525

    Google Scholar 

  • Verweyen HM, Karch H, Brandis B, Zimmerhackl LB (2000) Infections due to enterohemorrhagic E. coli: how to follow the routes of transmission. Pediatr Nephro114: 73–83

    Google Scholar 

  • International Collaborative Study Group for Bartter-like syndromes (1997) Mutations in the gene incoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. Hum Mol Genet 6: 17–26

    Google Scholar 

  • Rodriguez-Soriano J (1998) Bartter and related syndromes: the puzzle is almost solved. Ped Nephrol 12: 315–327

    Article  CAS  Google Scholar 

  • Simon DB, Nelson-Williams C, Bia MJ et al. (1996) Gitelman’s variant of Bartter syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet 12: 24–30

    Article  PubMed  CAS  Google Scholar 

  • Simon DB, Karet FE, Hamdan JM, Di Pietro A, Sanjad SA, Lifton RP (1996) Bartter’s syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2C1 cotransporter NKCC2. Nat Genet 13: 183–188

    Article  PubMed  CAS  Google Scholar 

  • Simon DB, Bindra R, Mansfield TA et al. (1997) Mutations in the chloride channel gene, CLCNKB, cause Bartter’s syndrome type III. Nat Genet 17: 171–178

    Google Scholar 

  • Vargas-Pousou R, Feldman D, Vollmer M et al. (1998) Novel molecular variants of the NaK2CL cotransporter gene are responsible for antenatal Bartter syndrome. Am J Hum Genet 62: 1332–1340

    Article  Google Scholar 

  • Vollmer M, Koehrer M, Topaloglu R, Strahm B, Omran H, Hildebrandt F (1998) Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome. Pediatr Nephro112: 69–71

    Google Scholar 

  • Goodyer P, Saadi I, Ong P, Elkas G, Rozen R (1998) Cystinuria subtype and the risk of nephrolithiasis. Kidney Int 54: 56–61

    Article  PubMed  CAS  Google Scholar 

  • Kelleher CL, Buckalew VM, Frederickson ED, Rhodes DJ, Conner DA, Seidman JG, Seidman CE (1998) CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets. Kidney Int 53: 31–37

    Article  PubMed  CAS  Google Scholar 

  • Longo JA, Netto Junior NR (1995) Extracorporeal shock-wave lithotripsy in children. Urology 46: 550–552

    Article  PubMed  CAS  Google Scholar 

  • Pierides AM (1997) Clinical aspects of cystinuria. Contrib Nephrol 122: 167–72

    Article  PubMed  CAS  Google Scholar 

  • Stapleton FB (1996) Clinical approach to children with urolithiasis. Semin Nephrol 16: 389–397

    PubMed  CAS  Google Scholar 

  • Trinchieri A, Rovera F, Nespoli R, Curro A (1996) Clinical observations on 2086 patients with upper urinary tract stone. Arch Ital Urol Androl 68: 251–262

    PubMed  CAS  Google Scholar 

  • Volpe P, Peyrottes A, Lammle M, Saquet D, Choquenet C (1997) Xanthine urinary calculus in a patient with Lesch-Nyhan syndrome. Apropos of a case. Prog Urol 7: 74–77

    Google Scholar 

  • Kwiatkowski DJ, Short MP (1994) Tuberous sclerosis. Arch Dermatol 130: 348–354

    Article  PubMed  CAS  Google Scholar 

  • Povey S, Burley AW, Attwood J et al. (1994) Two loci for tuberous sclero- sis. One on 9g34 and one on 16p13. Ann Hum Genet 58: 107–127

    Google Scholar 

  • Zimmerhackl LB, Rehm M, Kaufmehl K, Kurlemann G, Brandis M (1994) Renal involvement in tuberous sclerosis complex: a retrospective Friedman AL (1998) Urinary tract infection. Curr Opin Pediatr 10: 197–200

    Google Scholar 

  • Mannhardt W, Becker A, Putzer M, Bork M, Zepp F, Hacker J, SchulteWissermann H (1996) Host defense within the urinary tract. I. Bacterial adhesion initiates an uroepithelial defense mechanism. Pediatr Nephrol to: 568–572

    Google Scholar 

  • Marild S, Jodal U (1998) Incidence rate of first-time symptomatic urinary tract infection in children under 6 years of age. Acta Paediatr 87: 549–552

    Google Scholar 

  • Rosenfeld DL, Fleischer M, Yudd A, Makowsky T (1995) Current recommendations for children with urinary tract infections. Clin Pediatr 34: 261–264

    Google Scholar 

  • Rushton HG (1997) Urinary tract infections in children. Epidemiology, evaluation, and management. Pediatr Clin North Am 44: 1133–1169

    Article  PubMed  CAS  Google Scholar 

  • Schlager TA, Dilks S, Trudell J, Whittam TS, Hendley JO (1995) Bacteriuria in children with neurogenic bladder treated with intermittent catheterization: natural history. J Pediatr 126: 490–496

    Article  PubMed  CAS  Google Scholar 

  • Smellie JM, Rigden SP, Prescod NP (1995) Urinary tract infection: a Stapleton A, Stamm WE (1997) Prevention of urinary tract infection. In-comparison of four methods of investigation. Arch Dis Child 72: fect Dis Clin North Am 11: 719–733

    Google Scholar 

  • Arnell H (1998) The genetics of nocturnal enuresis: a simple question of complexity. Acta Paediatr. 87: 487–488

    Article  PubMed  CAS  Google Scholar 

  • Bradbury M (1997) Combination therapy for nocturnal enuresis with desmopressin and an alarm device. Scand J Urol Nephrol Supp1183: 61–63

    Google Scholar 

  • Combs AJ, Glassberg AD, Gerdes D, Horowitz M (1998) Biofeedback the- rapy for children with dysfunctional voiding. Urology 52: 312–315

    Article  PubMed  CAS  Google Scholar 

  • Hirasing RA, Leerdam FJ van, Bolk-Bennink LB, Bosch JD (1997) Bedwetting and behavioural and/or emotional problems. Acta Paediatr 86: 1131–1134

    Article  PubMed  CAS  Google Scholar 

  • Kawauchi A, Watanabe H, Miyoshi K (1996) Early morning urine osmolality in nonenuretic and enuretic children. Pediatr Nephrol 10: 696–698

    Article  PubMed  CAS  Google Scholar 

  • Norgaard JP, Gool JD van, Hjalmas K, Djurhuus JC, Hellstrom AL (1998) Standardization and definitions in lower urinary tract dysfunction in children. International Children’s Continence Society. Br J Urol 81 (Suppl 3): 1–16

    PubMed  Google Scholar 

  • Robson WL, Leung AK, Bloom DA (1996) Daytime wetting in childhood. Clin Pediatr (Phila) 35: 91–98

    Google Scholar 

  • Skoog SJ (1998) Behavior modification in the treatment of enuresis. J Urol 160: 861–862

    Article  PubMed  CAS  Google Scholar 

  • Wan J, Greenfield S (1997) Enuresis and common voiding abnormalities. Pediatr Clin North Am 44: 1117–1131

    Article  PubMed  CAS  Google Scholar 

  • Rascher W (1992) The hypertensive child. In: Cameron S, Davison AM, Grünfeld J-P, Kerr D, Ritz E (eds) Oxford textbook of clinical nephrology. Oxford Univ Press, Oxford, pp 2139–2152

    Google Scholar 

  • Sinaiko AR (1996) Hypertension in children. N Engl J Med 335: 1968–1973

    Article  PubMed  CAS  Google Scholar 

  • Working group from the National High Blood Pressure Education Program (1996) Update on the task force (1987) on high blood pressure in children and adolescents. Pediatrics 98: 649–658

    Google Scholar 

  • Flynn JT (1998) Causes, management approaches and outcome of acute renal failure in children. Curr Opin Pediatr 10: 184–189

    Article  PubMed  CAS  Google Scholar 

  • Hentschel R, Lodige B, Bulla M (1996) Renal insufficiency in the neonatal period. Clin Nephrol 46: 54–58

    PubMed  CAS  Google Scholar 

  • Warady BA, Bunchman TE (1996) An update on peritoneal dialysis and hemodialysis in the pediatric population. Curr Opin Pediatr 8: 135–140

    Article  PubMed  CAS  Google Scholar 

  • Zobel G, Rodl S, Urlesberger B, Kuttnig-Haim M, Ring E (1998) Conti-nous renal replacement therapy in critically ill patients. Kidney Int Suppl 66: 169–173

    Google Scholar 

  • Bulla M, Rosenkranz J (1996) 25 Jahre Nierenersatztherapie im Kindes-und Jugendlichenalter–Ein Erfolg der somatischen and psychosozialen Rehabilitation. Versicherungsmedizin 84: 85–89

    Google Scholar 

  • Fischbach M, Desprez P, Terzic J, Lahlou A, Mengus L, Geisert J (1996) Use of intraperitoneal pressure, ultrafiltration and purification dwell times for individual peritoneal dialysis prescription in children. Clin Nephrol 46: 14–16

    PubMed  CAS  Google Scholar 

  • Fivush BA, Jabs K, Neu AM, Sullivan EK, Feld L, Kohaut E, Fine R (1998) Chronic renal insufficiency in children and adolescents: the 1996 annual report of NAPRTCS. Pediatr Nephrol 12: 328–337

    Article  PubMed  CAS  Google Scholar 

  • Friedman AL (1996) Etiology, pathophysiology, diagnosis and management of chronic renal failure in children. Curr Opin Pediatr 8: 148–151

    Article  PubMed  CAS  Google Scholar 

  • Mehls O, Wühl E, Haffner D, Schäfer F, Tönshoff B (1996) Growth hormone treatment of short children with chronic renal failure before and after renal transplantation: rationale and recent results. Nephrol Dial Transplant u: 1747–1750

    Google Scholar 

  • Querfeld U, Michalk D (1995) Dialyse im Kindesalte. Pädiat Prax 49: 633–646

    Google Scholar 

  • Sedman A, Friedman A, Boineau F, Strife CF, Fine R (1996) Nutritional management of the child with mild to moderate chronic renal failure. J Pediatr 129: 13–18

    Google Scholar 

  • Davis ID, Bunchman TE, Grimm PC et al. (1998) Pediatric renal transplantation: indications and special considerations. A position paper from the Pediatric Committee of the American Society of Transplant Physicians. Pediatr Transplant 2 (2): 117–129

    PubMed  CAS  Google Scholar 

  • Gagnadoux MF, Niaudet P, Broyer M (1993) Non-immunological risk factors in paediatric renal transplantation. Pediatr Nephrol 7(1): 89-95

    Google Scholar 

  • Harmon WE, Dharnidharka VR (1999) Lymphoproliferative disease in children. Transplant Proc 31(1–2): 1268–1269

    Google Scholar 

  • Mehls O, Rigden S, Ehrich JH, Berthoux F, Jones EH, Valderrabano F (1996) Report on management of renal failure in Europe, XXV,1994. The child-adult interface. The EDTA-ERA Registry. European Dialysis and Transplant Association-European Renal Association. Nephrol Dial Transplant 11 (Suppl 1): 22–36

    Article  PubMed  Google Scholar 

  • Neu AM, Fivush BA (1998) Recommended immunization practices for pediatric renal transplant recipients. Pediatr Transplant 2 (4): 263–269

    PubMed  CAS  Google Scholar 

  • Warady BA, Alexander SR, Watkins S, Kohaut E, Harmon WE (1999) Optimal care of the pediatric end-stage renal disease patient on dialysis. Am J Kidney Dis 33 (3): 567–583

    Article  PubMed  CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2001 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Brandis, M., Hildebrandt, F., Zimmerhackl, L.B. (2001). Krankheiten der Niere, der ableitenden Harnwege und des äußeren Genitales. In: Lentze, M.J., Schaub, J., Schulte, F.J., Spranger, J. (eds) Pädiatrie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-12660-8_20

Download citation

  • DOI: https://doi.org/10.1007/978-3-662-12660-8_20

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-12661-5

  • Online ISBN: 978-3-662-12660-8

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics