Skip to main content
Top
Published in: Journal of Medical Case Reports 1/2018

Open Access 01-12-2018 | Case report

Bartter syndrome-like phenotype in a patient with diabetes: a case report

Authors: Chamara Dalugama, Manoji Pathirage, S. A. M. Kularatne

Published in: Journal of Medical Case Reports | Issue 1/2018

Login to get access

Abstract

Background

Bartter’s syndrome is a rare genetic tubulopathy affecting the loop of Henle leading to salt wasting. It is commonly seen in utero or in early neonatal period. Rare cases of acquired Bartter’s syndrome are reported in association with infections like tuberculosis, granulomatous conditions like sarcoidosis, autoimmune diseases, and drugs. The mainstay of management includes potassium, calcium, and magnesium supplementation.

Case presentation

We report the case of a 62-year-old Sri Lankan Sinhalese man with diabetes and hypertension presenting with generalized weakness with clinical evidence of proximal myopathy. He was severely hypokalemic with high urinary potassium excretion and hypochloremic metabolic alkalosis. He poorly responded to intravenously administered potassium supplements. A diagnosis of idiopathic Bartter-like phenotype was made. He responded well to spironolactone and indomethacin.

Conclusions

Patients presenting with body weakness need serum potassium estimation. Acquired Bartter’s syndrome although rare, should be ruled out in those with hypokalemia and metabolic alkalosis with increased urinary potassium loss with poor response to potassium replacement.
Literature
1.
go back to reference Bartter FC, Pronove P, Gill JR, MacCardle RC. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. Am J Med. 1962;33(6):811–28.CrossRefPubMed Bartter FC, Pronove P, Gill JR, MacCardle RC. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. Am J Med. 1962;33(6):811–28.CrossRefPubMed
2.
go back to reference Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet. 2008;40(5):592.CrossRefPubMedPubMedCentral Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. Rare independent mutations in renal salt handling genes contribute to blood pressure variation. Nat Genet. 2008;40(5):592.CrossRefPubMedPubMedCentral
3.
go back to reference Longo DL, Fauci AS, Kasper DL, Hauser SL, Jameson JL, Loscalzo S. Harrison’s Principles of Internal Medicine, vol. 2. 18th ed. USA: The McGraw Hill Companies; 2012. p. 2360–1. Longo DL, Fauci AS, Kasper DL, Hauser SL, Jameson JL, Loscalzo S. Harrison’s Principles of Internal Medicine, vol. 2. 18th ed. USA: The McGraw Hill Companies; 2012. p. 2360–1.
4.
go back to reference Gadwalkar SR, Murthy PR, Raghavendra, Nandini K, Deepa DV. Acquired Bartter-Like Phenotype. J Assoc Physicians India. 2015;63(9):78–9.PubMed Gadwalkar SR, Murthy PR, Raghavendra, Nandini K, Deepa DV. Acquired Bartter-Like Phenotype. J Assoc Physicians India. 2015;63(9):78–9.PubMed
5.
go back to reference Simon DB, Karet FE, Hamdan JM, et al. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet. 1996;13:183.CrossRefPubMed Simon DB, Karet FE, Hamdan JM, et al. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet. 1996;13:183.CrossRefPubMed
6.
go back to reference Simon DB, Karet FE, Rodriguez-Soriano J, et al. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK. Nat Genet. 1996;14:152.CrossRefPubMed Simon DB, Karet FE, Rodriguez-Soriano J, et al. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK. Nat Genet. 1996;14:152.CrossRefPubMed
7.
go back to reference Simon DB, Bindra RS, Mansfield TA, et al. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet. 1997;17:171.CrossRefPubMed Simon DB, Bindra RS, Mansfield TA, et al. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet. 1997;17:171.CrossRefPubMed
8.
go back to reference Konrad M, Vollmer M, Lemmink HH, et al. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol. 2000;11:1449.PubMed Konrad M, Vollmer M, Lemmink HH, et al. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol. 2000;11:1449.PubMed
9.
go back to reference Schlingmann KP, Konrad M, Jeck N, et al. Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med. 2004;350:1314.CrossRefPubMed Schlingmann KP, Konrad M, Jeck N, et al. Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med. 2004;350:1314.CrossRefPubMed
10.
go back to reference Stoian M, Chitac D, Bontas E, Dumitrescu AM, Stocia V. Bartter syndrome with pulmonary Tuberculosis a shortly outlook. Med J Clin Med. 2007;2:332–6. Stoian M, Chitac D, Bontas E, Dumitrescu AM, Stocia V. Bartter syndrome with pulmonary Tuberculosis a shortly outlook. Med J Clin Med. 2007;2:332–6.
11.
go back to reference Workeneh B, Sangsiraprabha W, Addison D, Longfield E. A novel case of persistent bartters-like syndrome associated with gentamycin exposure. Saudi J Kidney Dis Transpl. 2013;24:144–6.CrossRefPubMed Workeneh B, Sangsiraprabha W, Addison D, Longfield E. A novel case of persistent bartters-like syndrome associated with gentamycin exposure. Saudi J Kidney Dis Transpl. 2013;24:144–6.CrossRefPubMed
12.
go back to reference Chrispal A, Boorugu H, Prabhakar AT, Moses V. Amikacin-induced type 5 Bartter-like syndrome with severe hypocalcemia. J Postgrad Med. 2009;55:208–10.CrossRefPubMed Chrispal A, Boorugu H, Prabhakar AT, Moses V. Amikacin-induced type 5 Bartter-like syndrome with severe hypocalcemia. J Postgrad Med. 2009;55:208–10.CrossRefPubMed
14.
go back to reference López Sastre JB, CotoCotallo GD, Fernández Colomer B. Neonatal invasive candidiasis: a prospective multicenter study of 118 cases. Am J Perinatol. 2003;20(3):153–63.CrossRefPubMed López Sastre JB, CotoCotallo GD, Fernández Colomer B. Neonatal invasive candidiasis: a prospective multicenter study of 118 cases. Am J Perinatol. 2003;20(3):153–63.CrossRefPubMed
15.
go back to reference Miyata M, Takase Y, Kobayashi H, et al. Primary Sjogren’s syndrome complicated by sarcoidosis. Intern Med. 1998;37:174–8.CrossRefPubMed Miyata M, Takase Y, Kobayashi H, et al. Primary Sjogren’s syndrome complicated by sarcoidosis. Intern Med. 1998;37:174–8.CrossRefPubMed
16.
go back to reference Yu T-M, Lin S-H, Ya-Wen C, Wen M-C, Chen Y-H, Cheng C-H, Chen C-H, Chin C-S, Shu K-H. A syndrome resembling Bartter’s syndrome in sarcoidosis. Nephrol Dial Transplant. 2009;24:667–9.CrossRefPubMed Yu T-M, Lin S-H, Ya-Wen C, Wen M-C, Chen Y-H, Cheng C-H, Chen C-H, Chin C-S, Shu K-H. A syndrome resembling Bartter’s syndrome in sarcoidosis. Nephrol Dial Transplant. 2009;24:667–9.CrossRefPubMed
17.
go back to reference Muther RS, McCarron DA, Bennett WM. Granulomatous sarcoid nephritis: a cause of multiple renal tubular abnormalities. Clin Nephrol. 1980;14:190–7.PubMed Muther RS, McCarron DA, Bennett WM. Granulomatous sarcoid nephritis: a cause of multiple renal tubular abnormalities. Clin Nephrol. 1980;14:190–7.PubMed
18.
go back to reference Venkat Raman G, Albano JD, Millar JG, Lee HA. Bartter’s syndrome and diabetes mellitus. J Intern Med. 1990;228:525–31.CrossRefPubMed Venkat Raman G, Albano JD, Millar JG, Lee HA. Bartter’s syndrome and diabetes mellitus. J Intern Med. 1990;228:525–31.CrossRefPubMed
19.
go back to reference See TT, Lee SP. Bartter's syndrome with type 2 diabetes mellitus. J Chin Med Assoc. 2009;72(2):88–90.CrossRefPubMed See TT, Lee SP. Bartter's syndrome with type 2 diabetes mellitus. J Chin Med Assoc. 2009;72(2):88–90.CrossRefPubMed
20.
go back to reference Zillich AJ, Garg J, Basu S, Bakris GL, Carter BL. Thiazide diuretics, potassium, and the development of diabetes: a quantitative review. Hypertension. 2006;48:219–24.CrossRefPubMed Zillich AJ, Garg J, Basu S, Bakris GL, Carter BL. Thiazide diuretics, potassium, and the development of diabetes: a quantitative review. Hypertension. 2006;48:219–24.CrossRefPubMed
21.
go back to reference Rodríguez-Soriano J. Bartter and related syndromes; the puzzle is almost solved. PediatrNephrol. 1998;12:315–27. Rodríguez-Soriano J. Bartter and related syndromes; the puzzle is almost solved. PediatrNephrol. 1998;12:315–27.
23.
go back to reference Hene RJ, Koomans HA, DorhoutMees EJ, Stople A, Verhoef GEG, Boer P. Correction of hypokalemia in Bartter's syndrome by enalapril. Am J Kidney. 1987;9:200–5.CrossRef Hene RJ, Koomans HA, DorhoutMees EJ, Stople A, Verhoef GEG, Boer P. Correction of hypokalemia in Bartter's syndrome by enalapril. Am J Kidney. 1987;9:200–5.CrossRef
24.
go back to reference Kleta R, Basoglu C, Kuwertz-Broking E. New treatment options for Bartter's syndrome. N Engl J Med. 2000;343:661–2.CrossRefPubMed Kleta R, Basoglu C, Kuwertz-Broking E. New treatment options for Bartter's syndrome. N Engl J Med. 2000;343:661–2.CrossRefPubMed
Metadata
Title
Bartter syndrome-like phenotype in a patient with diabetes: a case report
Authors
Chamara Dalugama
Manoji Pathirage
S. A. M. Kularatne
Publication date
01-12-2018
Publisher
BioMed Central
Published in
Journal of Medical Case Reports / Issue 1/2018
Electronic ISSN: 1752-1947
DOI
https://doi.org/10.1186/s13256-018-1752-6

Other articles of this Issue 1/2018

Journal of Medical Case Reports 1/2018 Go to the issue