Bartter syndrome differential diagnosis: Difference between revisions

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| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Cystic fibrosis]]'''
| style="padding: 5px 5px; background: #DCDCDC;" | '''[[Cystic fibrosis]]'''
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*Patients with cystic fibrosis lose salt-rich sweat.  
*Patients with [[cystic fibrosis]] lose salt-rich sweat.  
*Patients with moderate cystic fibrosis manifest with unexplained hypokalemia and metabolic alkalosis.<ref name="pmid17323076">{{cite journal| author=Kose M, Pekcan S, Ozcelik U, Cobanoglu N, Yalcin E, Dogru D | display-authors=etal| title=An epidemic of pseudo-Bartter syndrome in cystic fibrosis patients. | journal=Eur J Pediatr | year= 2008 | volume= 167 | issue= 1 | pages= 115-6 | pmid=17323076 | doi=10.1007/s00431-007-0413-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17323076  }} </ref><ref name="pmid2386386">{{cite journal| author=Kennedy JD, Dinwiddie R, Daman-Willems C, Dillon MJ, Matthew DJ| title=Pseudo-Bartter's syndrome in cystic fibrosis. | journal=Arch Dis Child | year= 1990 | volume= 65 | issue= 7 | pages= 786-7 | pmid=2386386 | doi=10.1136/adc.65.7.786 | pmc=1792454 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2386386  }} </ref><ref name="pmid9048354">{{cite journal| author=Bates CM, Baum M, Quigley R| title=Cystic fibrosis presenting with hypokalemia and metabolic alkalosis in a previously healthy adolescent. | journal=J Am Soc Nephrol | year= 1997 | volume= 8 | issue= 2 | pages= 352-5 | pmid=9048354 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9048354  }} </ref>  
*Patients with moderate [[cystic fibrosis]] manifest with unexplained [[hypokalemia]] and [[metabolic alkalosis]].<ref name="pmid17323076">{{cite journal| author=Kose M, Pekcan S, Ozcelik U, Cobanoglu N, Yalcin E, Dogru D | display-authors=etal| title=An epidemic of pseudo-Bartter syndrome in cystic fibrosis patients. | journal=Eur J Pediatr | year= 2008 | volume= 167 | issue= 1 | pages= 115-6 | pmid=17323076 | doi=10.1007/s00431-007-0413-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17323076  }} </ref><ref name="pmid2386386">{{cite journal| author=Kennedy JD, Dinwiddie R, Daman-Willems C, Dillon MJ, Matthew DJ| title=Pseudo-Bartter's syndrome in cystic fibrosis. | journal=Arch Dis Child | year= 1990 | volume= 65 | issue= 7 | pages= 786-7 | pmid=2386386 | doi=10.1136/adc.65.7.786 | pmc=1792454 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2386386  }} </ref><ref name="pmid9048354">{{cite journal| author=Bates CM, Baum M, Quigley R| title=Cystic fibrosis presenting with hypokalemia and metabolic alkalosis in a previously healthy adolescent. | journal=J Am Soc Nephrol | year= 1997 | volume= 8 | issue= 2 | pages= 352-5 | pmid=9048354 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9048354  }} </ref>  
*In contrast to Bartter syndrome, spot urine chloride concentration is low in cystic fibrosis indicating chloride conservation in response to volume contraction.<ref name="pmid15754262">{{cite journal| author=Davé S, Honney S, Raymond J, Flume PA| title=An unusual presentation of cystic fibrosis in an adult. | journal=Am J Kidney Dis | year= 2005 | volume= 45 | issue= 3 | pages= e41-4 | pmid=15754262 | doi=10.1053/j.ajkd.2004.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15754262  }} </ref><ref name="pmid7543567">{{cite journal| author=Leoni GB, Pitzalis S, Podda R, Zanda M, Silvetti M, Caocci L | display-authors=etal| title=A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydration. | journal=J Pediatr | year= 1995 | volume= 127 | issue= 2 | pages= 281-3 | pmid=7543567 | doi=10.1016/s0022-3476(95)70310-1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7543567  }} </ref>
*In contrast to [[Bartter syndrome]], spot urine [[chloride]] concentration is low in [[cystic fibrosis]] indicating [[chloride]] conservation in response to volume contraction.<ref name="pmid15754262">{{cite journal| author=Davé S, Honney S, Raymond J, Flume PA| title=An unusual presentation of cystic fibrosis in an adult. | journal=Am J Kidney Dis | year= 2005 | volume= 45 | issue= 3 | pages= e41-4 | pmid=15754262 | doi=10.1053/j.ajkd.2004.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15754262  }} </ref><ref name="pmid7543567">{{cite journal| author=Leoni GB, Pitzalis S, Podda R, Zanda M, Silvetti M, Caocci L | display-authors=etal| title=A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydration. | journal=J Pediatr | year= 1995 | volume= 127 | issue= 2 | pages= 281-3 | pmid=7543567 | doi=10.1016/s0022-3476(95)70310-1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7543567  }} </ref>
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| style="padding: 5px 5px; background: #DCDCDC;" | '''Gullner syndrome - Familial hypokalemic alkalosis with proximal tubulopathy'''
| style="padding: 5px 5px; background: #DCDCDC;" | '''Gullner syndrome - Familial hypokalemic alkalosis with proximal tubulopathy'''

Revision as of 11:54, 31 July 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Tayyaba Ali, M.D.[2]

Overview

Differentiating Bartter syndrome from other Diseases

Bartter syndrome diagnosis should be differentiated from other diseases manifesting with hypokalemia and hypochloremic metabolic alkalosis.[1]

Disease Findings
Gitelman syndrome
Diuretic abuse
Cyclical vomiting
Hyperprostaglandin E syndrome
Familial hypomagnesemia with hypercalciuria/nephrocalcinosis
Cystic fibrosis
Gullner syndrome - Familial hypokalemic alkalosis with proximal tubulopathy
Mineralocorticoid excess
Activating mutations of the CaSR calcium-sensing receptor
Hypomagnesemia
Congenital chloride diarrhea
Hypochloremic alkalosis
Hypokalemia

References

  1. Gitelman HJ, Graham JB, Welt LG (1966). "A new familial disorder characterized by hypokalemia and hypomagnesemia". Trans Assoc Am Physicians. 79: 221–35. PMID 5929460.
  2. Scognamiglio R, Negut C, Calò LA (2007). "Aborted sudden cardiac death in two patients with Bartter's/Gitelman's syndromes". Clin Nephrol. 67 (3): 193–7. doi:10.5414/cnp67193. PMID 17390745.
  3. Urbanová M, Reiterová J, Stěkrová J, Lněnička P, Ryšavá R (2011). "DNA analysis of renal electrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes: summary of mutation screening". Folia Biol (Praha). 57 (2): 65–73. PMID 21631963.
  4. Jamison RL, Ross JC, Kempson RL, Sufit CR, Parker TE (1982). "Surreptitious diuretic ingestion and pseudo-Bartter's syndrome". Am J Med. 73 (1): 142–7. doi:10.1016/0002-9343(82)90941-x. PMID 7091169.
  5. Colussi G, Rombolà G, Airaghi C, De Ferrari ME, Minetti L (1992). "Pseudo-Bartter's syndrome from surreptitious diuretic intake: differential diagnosis with true Bartter's syndrome". Nephrol Dial Transplant. 7 (9): 896–901. doi:10.1093/ndt/7.9.896. PMID 1328936.
  6. Sasaki H, Kawasaki T, Yamamoto T, Ninomiya H, Ono J, Yamamoto T; et al. (1986). "[Pseudo-Bartter's syndrome induced by surreptitious ingestion of furosemide to lose weight: a case report and possible pathophysiology]". Nihon Naibunpi Gakkai Zasshi. 62 (8): 867–81. doi:10.1507/endocrine1927.62.8_867. PMID 3023152.
  7. D'Avanzo M, Santinelli R, Tolone C, Bettinelli A, Bianchetti MG (1995). "Concealed administration of frusemide simulating Bartter syndrome in a 4.5-year-old boy". Pediatr Nephrol. 9 (6): 749–50. doi:10.1007/BF00868731. PMID 8747119.
  8. Veldhuis JD, Bardin CW, Demers LM (1979). "Metabolic mimicry of Bartter's syndrome by covert vomiting: utility of urinary chloride determinations". Am J Med. 66 (2): 361–3. doi:10.1016/0002-9343(79)90566-7. PMID 425977.
  9. Kose M, Pekcan S, Ozcelik U, Cobanoglu N, Yalcin E, Dogru D; et al. (2008). "An epidemic of pseudo-Bartter syndrome in cystic fibrosis patients". Eur J Pediatr. 167 (1): 115–6. doi:10.1007/s00431-007-0413-3. PMID 17323076.
  10. Kennedy JD, Dinwiddie R, Daman-Willems C, Dillon MJ, Matthew DJ (1990). "Pseudo-Bartter's syndrome in cystic fibrosis". Arch Dis Child. 65 (7): 786–7. doi:10.1136/adc.65.7.786. PMC 1792454. PMID 2386386.
  11. Bates CM, Baum M, Quigley R (1997). "Cystic fibrosis presenting with hypokalemia and metabolic alkalosis in a previously healthy adolescent". J Am Soc Nephrol. 8 (2): 352–5. PMID 9048354.
  12. Davé S, Honney S, Raymond J, Flume PA (2005). "An unusual presentation of cystic fibrosis in an adult". Am J Kidney Dis. 45 (3): e41–4. doi:10.1053/j.ajkd.2004.11.009. PMID 15754262.
  13. Leoni GB, Pitzalis S, Podda R, Zanda M, Silvetti M, Caocci L; et al. (1995). "A specific cystic fibrosis mutation (T3381) associated with the phenotype of isolated hypotonic dehydration". J Pediatr. 127 (2): 281–3. doi:10.1016/s0022-3476(95)70310-1. PMID 7543567.


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