Diagnosis and treatment of renal tubular disorders

Seminars in Nephrology

Volumn 18, Issue 3, 1998, Pages 317-329

  Gregory, Melissa J ^a   Schwartz, George J ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; CAPTOPRIL; CISPLATIN; CITRIC ACID; GENTAMICIN; IBUPROFEN; IFOSFAMIDE; MAGNESIUM; PENICILLAMINE; PHOSPHATE; POTASSIUM; PROSTAGLANDIN INHIBITOR; SPIRONOLACTONE; STREPTOZOCIN; TIOPRONIN; VALPROIC ACID; VITAMIN D;

ACID BASE BALANCE; AMINOACIDURIA; BARTTER SYNDROME; BONE MARROW TOXICITY; CLINICAL FEATURE; DIAGNOSTIC APPROACH ROUTE; DIFFERENTIAL DIAGNOSIS; ELECTROLYTE DISTURBANCE; FANCONI RENOTUBULAR SYNDROME; FLUID BALANCE; GASTROINTESTINAL DISEASE; GITELMAN SYNDROME; GROWTH RETARDATION; HUMAN; INTRAVENOUS DRUG ADMINISTRATION; KIDNEY TUBULE ACIDOSIS; KIDNEY TUBULE DISORDER; NEPHROTIC SYNDROME; ORAL DRUG ADMINISTRATION; PATHOPHYSIOLOGY; POLYMYOSITIS; PRACTICE GUIDELINE; PRIORITY JOURNAL; REVIEW;

ACIDOSIS, RENAL TUBULAR; CHILD; FANCONI SYNDROME; HUMANS; KIDNEY DISEASES; KIDNEY TUBULES;

EID: 0031966380     PISSN: 02709295     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (73)

1. Donckerwolcke RA: Diagnosis and treatment of renal tubular disorders in children. Pediatr Clin North Am 29:895-906, 1982
2. Foreman J: Fanconi syndrome and cystinosis, in Holliday MA, Barratt TM, Avner ED (eds): Pediatric Nephrology. Baltimore, MD, Williams &Wilkins, 1994, pp 537-557
3. Eiam-ong S, Spohn M, Kurtzman NA, Sabatini S: Insights into the biochemical mechanism of maleic acid-induced Fanconi syndrome. Kidney Int 48:1542-1548, 1995
4. Bovee KC, Joyce T, Reynolds R, Segal S: The Fanconi syndrome in Basenji dogs: A new model for renal transport defects. Science 201:1129-1131, 1978
5. Rossi RM, Kist C, Wurster U, et al: Estimation of ifosfamide/cisplatinum-induced renal toxicity by urinary protein analysis. Pediatr Nephrol 8:151-156, 1994
6. Heney D, Wheeldon J, Rushworth P, et al: Progressive renal toxicity due to ifosfamide. Arch Dis Child 66:966-770, 1991
7. Skinner R, Sharkey IM, Pearson ADJ, Craft AW: Ifosfamide, mesna, and nephrotoxicity in children. J Clin Oncol 11:173-190, 1993
8. Goren MP, Wright RK, Horowitz ME, Pratt CB: Ifosfamide-induced subclinical tubular nephrotoxicity despite mesna. Cancer Treat Rep 71:127-130, 1987
9. Burk CD, Restaino I, Kaplan BS, Meadows AT: Ifosfamide-induced renal tubular dysfunction and rickets in children with Wilms tumor. J Pediatr 117:331-335, 1990
10. Houston IB, Boichis H, Edelmann CM Jr: Fanconi syndrome with renal sodium wasting and metabolic alkalosis. Am J Med 44:638-646, 1968
11. Luder J, Sheldon WA: Familial tubular absorption defect of glucose and amino acids. Arch Dis Child 30:160-164, 1955
12. Lande MB, Kim MS, Bartlett C, et al: Reversible Fanconi syndrome associated with valproate therapy. J Pediatr 123:320-322, 1993
13. Melnick JZ, Baum M, Thompson JR: Aminoglycoside-induced Fanconi's syndrome. Am J Kidney Dis 23:118-122, 1994
14. Rutchik SD, Resnick MI: Cystine calculi. Diagnosis and management Urol Clin North Am 24:163-171, 1997
15. Smith A, Wilcken B: Homozygous cystinuria in New South Wales. A study of 110 individuals with cystinuria ascertained by methods other than neonatal screening. Med J Aust 141:500-502, 1984
16. Weinberger A, Sperling O, Rabinovitz M, et al: High frequency of cystinuria among Jews of Libyan origin. Human Heredity 24:568-572, 1974
17. Gitomer WL, Pad CYC: Recent advances in the biochemical and molecular biochemical basis of cystinuria. J Urol 156:1907-1912, 1996
18. Sakhaee K: Cystinuria: Pathogenesis and treatment. Miner Electrolyte Metab 20:414-423, 1994
19. Foreman JW, Hwang SM, Segal S: Transport interactions of cystine and dibasic amino acids in isolated rat renal tubules. Metabolism 29:53-61, 1980
20. Singer A, Das S: Cystinuria: A review of the pathophysiology and management. J Urol 142:669-673, 1989
21. Dent LE, Friedman M, Green H, Watson LCA: Treatment of cystinuria. Br Med J 1:403-408, 1965
22. Rodriguez LM, Santos F, Malaga S.'Martinez V: Effect of a low sodium diet on urinary elimination of cystine in cystinuric children. Nephron 71:416-418, 1995
23. Chow GK, Streem SB: Medical treatment of cystinuria: Results of contemporary clinical practice. J Urol 156:1576-1578, 1996
24. Lindell A, Denneberg T, Hellgren E, et al: Clinical course and cystine stone formation during tiopronin treatment. Urol Res 23:111-117, 1995
25. Pak CYC, Fuller C, Sakhaee K, et al: Management of cystine nephrolithiasis with alpha-mercaptopropionylglycine. J Urol 136:1003-1008, 1986
26. Cohen TD, Streem SB, Hall P: Clinical effect of captopril on the formation and growth of cystine calculi. J Urol 154:164-166, 1995
27. Michelakakis H, Delis D, Anastasiadou V, Bartsocas C: Ineffectiveness of captopril in reducing cystine excretion in cystinuric children. J Inher Metab Dis 16:1042-1043, 1993
28. Alpern RJ, Stone DK, Rector FC Jr: Renal acidification mechanisms, in Brenner BM, Rector RC Jr (eds): The Kidney. Philadelphia, PA, Saunders, 1991, pp 318-379
29. Sabatini S, Kurtzman NA: Overall acid-base regulation by the kidney, in Seldin DW, Giebisch G (eds): Regulation of Acid-Base Balance. New York, NY, Raven Press, 1989, pp 185-210
30. Schwartz GJ: General principles of acid-base physiology, in Holliday MA, Barratt TM, Avner ED (eds): Pediatric Nephrology. Baltimore, MD, Williams & Wilkins, 1994, pp 222-246
31. Dubose TD Jrf, Good DW, Hamm LL, Wall SM: Ammonium transport in the kidney: New physiological concepts and their clinical implications. J Am Soc Nephrol 1:1193-1203, 1991
32. Rodriguez-Soriano J, Boichis H, Stark H, Edelmann CM: Proximal renal tubular acidosis. A defect in bicarbonate reabsorption with normal urinary acidification. Pediatr Res 1:81-98, 1967
33. Brenes LG, Brenes JN, Hernandez MM: Familial proximal renal tubular acidosis. A distinct clinical entity. Am J Med 63:244-252, 1977
34. Rodriguez-Soriano J, Vallo A: Renal tubular acidosis. Pediatr Nephrol 4:268-275, 1990
35. Lemann J Jr, Wilz DR, Brenes LG: Acid, calcium and phosphorous balance in proximal renal tubular acidosis. Kidney Int 10:561A, 1976 (abstr)
36. Brenes LG, Sanchez MI: Impaired urinary ammonium excretion in patients with isolated proximal renal tubular acidosis. J Am Soc Nephrol 4:1073-1078, 1993
37. Smulders YM, Frissen PHJ, Slaats EH, Silberbusch J: Renal tubular acidosis. Pathophysiology and diagnosis. Arch Intern Med 156:1629-1636, 1996
38. Gluck SL, lyori M, Holliday LS, et al: Distal urinary acidification from Homer Smith to present. Kidney Int 49:1660-1664, 1996
39. Laski ME, Kurtzman NA: Characterization of acidification in the cortical and medullary collecting tubule of the rabbit. J Clin Invest 72:2050-2059, 1983
40. Schwanz JH: Renal acid-base transport: The regulatory role of the inner medullary collecting duct. Kidney Int 47:333-341, 1995
41. Wingo CS, Cain BD: The renal H-K-ATPase: Physiological significance and role in potassium homeostasis. Annu Rev Physiol 55:323-347, 1993
42. Rodriguez-Soriano J, Vallo A, Garcia-Fuentes M: Distal renal tubular acidosis in infancy: A bicarbonate wasting state. J Pediatr 86:524-532, 1975
43. Kurtzman NA: Disorders of distal acidification. Kidney Int 38:720-727, 1990
44. Baille D, Flores G: Underlying defects in distal renal tubular acidosis: New understandings. Am J Kidney Dis 27:896-915, 1996
45. Caldas A, Broyer M, Dechaux M, Kleinknecht C: Primary distal tubular acidosis in childhood: Clinical study and long-term follow-up of 28 patients. J Pediatr 121:233-241, 1992
46. Guizar JM, Komhauser C, Malacara JM, et al: Renal tubular acidosis in children with vesicoureteral reflux. J Urol 156:193-195, 1996
47. Portale AA: Renal tubular acidosis, in Holliday MA, Barratt TM, Avner ED (eds): Pediatric Nephrology. Baltimore, MD, Williams &Wilkins, 1994, pp 640-662
48. Zelikovic I: Renal tubular acidosis. Pediatr Annal 24:48-54, 1995
49. Miller SG, Schwanz GJ: Hyperammonaemia with distal renal tubular acidosis. Arch Dis Child 77:441-444, 1997
50. Carlisle EJF, Donnelly SM, Halperin ML: Renal tubular acidosis (RTA): Recognize The Ammonium defect and pHorget the urine pH. Pediatr Nephrol 5:242-248, 1991
51. Battle DC, Hizon M, Cohen E, et al: The use of the urinary anion gap in the diagnosis of hyperchloremic metabolic acidosis. N EngI J Med 318:594-599, 1988
52. Edelmann CM Jr, Rodriguez-Soriano J, Boichis H, et al: Renal bicarbonate reabsorption and hydrogen ion excretion in normal infants. J Clin Invest 46:1309-1317, 1967
53. Katz AI: Renal Na-K-ATPase: Its role in tubular sodium and potassium transport. Am J Physiol (Renal Fluid Electrolyte Physiol 11) 242:F207-F219, 1982
54. O'Neil RG, Sansom SC: Characterization of apical cell membrane Na and K conductances of cortical collecting tubule using microelectrode techniques. Am J Physiol (Renal Fluid Electrolyte Physiol 16) 247:F14-F24, 1984
55. Banter FC, Pronove P, Gill JR, Jr, MacCardle RC: Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. Am J Med 33:811-828, 1962
56. McCredic DA: Variants of Banter's syndrome. Pediatr Nephrol 10:419-421, 1996
57. Simon DB, Karet FE, Hamdan JM, et al: Banter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nature Genet 13:183-188, 1996
58. Simon DB, Lifton RP: The molecular basis of inherited hypokalemic alkalosis: Banter's and Gitelman's syndromes. Am J Physiol (Renal Fluid Electrolyte Physiol 40) 271:F961-F966, 1996
59. International Collaborative Study Group for Bartter-like Syndromes: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity. Hum Molec Genet 6:17-26, 1997
60. Seyberth HW, Rascher W, Schweer H, et al: Congential hypokalemia with hypercalciuria in preterm infants: A hyperprostaglandinuric tubular syndrome different from Bartter syndrome. J Pediatr 107:694-701, 1985
61. Seyberth HW: How can you differentiate neonatal Banter's syndrome from hyperprostaglandin (-uria) E2 syndrome. Pediatr Nephrol 8:407, 1994
62. Karolyi L, Ziegler A, Pollak M, et al: Gitelman's syndrome is genetically distinct from other forms of Banter's syndrome. Pediatr Nephrol 10:551-554, 1996
63. Pollak MR, Delaney VB, Graham, Hebert SC: Gitelman's syndrome (Banter's variant) maps to the thiazide-sensitive cotransporter gene locus on chromosome 16q13 in a large kindred. J Am Soc Nephrol 10:2244-2248, 1996
64. Simon DB, Nelson-Williams C, Bia MJ, et al: Gitelman's variant of Banter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive NaCl cotransporter. Nature Genet 12:24-30, 1996
65. Luthy C, Bettinelli A, Iselin S, et al: Normal prostaglandinuria in Gitelman's syndrome, the hypocalciuric variant of Banter's syndrome. Am J Kidney Dis 25:824-828, 1995
66. Clive DM: Banter's syndrome: The unsolved puzzle. Am J Kidney Dis 25:813-823, 1995
67. Mace JW, Hambidge M, Gotlin RW, et al: Magnesium supplementation in Banter's syndrome. Arch Dis Child 48:485-487, 1973
68. Meyer WJ III, Gill JR Jr, Banter FC: Gout as a complication of Banter's syndrome. A possible role for alkalosis in the decreased clearance of uric acid. Ann Intern Med 83:56-59, 1975
69. Bettinelli A, Bianchetti MG, Girardin E, et al: Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Banter and Gitelman syndromes. J Pediatr 120:38-43, 1992
70. Suki WN, Rouse D: Renal transport of calcium, magnesium, and phosphorus, in Brenner BM, Rector RC Jr (eds): The Kidney. Philadelphia, PA, Saunders, 1991, pp 380-423
71. Veldhuis JD, Bardin CW, Deniers LM: Metabolic mimicry of Banter's syndrome by covert vomiting. Utility of urinary chloride determination. Am J Med 66:361-363, 1979
72. Rodriguez-Soriano J: Tubular disorders of electrolyte regulation, in Holliday MA, Barratt TM, Avner ED (eds): Pediatric Nephrology. Baltimore, MD, Williams &Wilkins, 1994, pp 624-639
73. Mackic FE, Hodson EM, Roy LP, Knight JF: Neonatal Bartter syndrome-Use of indomethacin in the newborn period and prevention of growth failure. Pediatr Nephrol 10:756-758, 1996