- A Case of Atypical Gitelman's Syndrome with Normomagnesemia and Normal Magnesium Excretion
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Jeon JS, Kim YM, Noh H, Han DC
- KMID: 2254316
- Korean J Nephrol.
- 2004 Jul;23(4):626-629.
Gitelman's sydnrome is a heritable renal disorder characterized by hypomagnesemia, hypokalemia and hypocalciuria. As compared to those with Bartter's syndrome, reduced urinary excretion of calcium and magesium wasting are essential... -
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- Acquired Gitelman Syndrome
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Kim YK, Song HC, Kim YS, Choi EJ
- KMID: 1464782
- Electrolyte Blood Press.
- 2009 Jun;7(1):5-8.
- doi: 10.5049/EBP.2009.7.1.5
Acquired renal tubular disorder can be observed in various disease processes, especially autoimmune diseases. Gitelman syndrome is an autosomal recessive disease characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. This... -
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- Familial Gitelman Syndrome in Sisters
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Hong EJ, Ha TS
- KMID: 2254136
- Korean J Nephrol.
- 2007 Jan;26(1):102-106.
Gitelman syndrome is a hereditary renal tubular disorder characterized by hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. This syndrome is caused by the genetic mutation of SLC12A3 gene encoding thiazide-sensitive sodium-chloride... -
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- A Case of Gitelman's Syndrome Presented with Chest Pain and Syncope
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Shin HS, Park CH
- KMID: 1867705
- Korean J Nephrol.
- 2006 Nov;25(6):1013-1017.
Gitelman's syndrome is a rare autosomal recessive, inherited renal tubular disorder, first described by Gitelman et al. in 1966, and it is characterized by hypokalemic metabolic alkalosis, hypomagnesemia, salt wasting,... -
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- A Case of Gitelman's Like Syndrome Presenting with Rhabdomyolysis
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Lee J, Lee SH, Park YJ, Jo HS, Oh SH, Shin SJ, Kim YS, Cahng YS, Bang BK
- KMID: 2254171
- Korean J Nephrol.
- 2006 Mar;25(2):311-315.
Gitelman syndrome is an autosomal recessive hereditary disorder characterized by hypokalemic metabolic alkalosis, hypomagnesemia, salt wasting, low blood pressure, and hypocalciuria. Gitelman's syndrome is generally considered to be benign, and... -
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- A Case of Gitelman Syndrome
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Han YJ, Yeon EK, Kim YC
- KMID: 2317667
- Soonchunhyang Med Sci.
- 2012 Dec;18(2):145-147.
Gitelman's syndrome is an autosomal recessive disorder characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria that has recently been reported to be linked to thiazide-sensitive Na-Cl cotransporter gene mutation. We... -
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- HELLP syndrome in a pregnant patient with Gitelman syndrome
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Lee M, Kim DI, Lee KH, Byun JH, Hwang J, Hwang WM, Yun SR, Yoon SH
- KMID: 2409394
- Kidney Res Clin Pract.
- 2017 Mar;36(1):95-99.
- doi: 10.23876/j.krcp.2017.36.1.95
Gitelman syndrome is characterized by hypokalemia, metabolic alkalosis, hypocalciuria, and hypomagnesemia. The clinical course of Gitelman syndrome in pregnant women remains unclear, but it is thought to be benign. We... -
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- A Case of Pseudo-Gitelman's Syndrome Misdiagnosed as Gitelman's Syndrome
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Lee DK, Jung JM, Kang JG, Kim TY, Kim TJ, Oh HS, Choi CY, Han SW, Kim HJ
- KMID: 2254443
- Korean J Nephrol.
- 2002 May;21(3):475-480.
A 31-year-old woman had a history of fatigue and hypokalemia and metabolic alkalosis and hypocalciuria. The patient had a subtotal thyroidectomy and denied ingestion of diuretic medication. Her clinical and... -
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- The Effects of Magnesium Supplementation for Correcting Hypokalemia in Gitelman Syndrome
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Moon JD, Han SW, Kim HJ
- KMID: 2254158
- Korean J Nephrol.
- 2006 Mar;25(2):213-220.
BACKGOUND: Gitelman's syndrome is manifested by hypokalemia, metabolic alkalosis, normal blood pressure, hyperreninemic hyperaldosteronism, hypomagnesemia and hypocalciuria. This study was carried out to investigate the effects of magnesium supplementation for... -
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- A Case of Gitelman's Syndrome
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Cha YH, Song MJ, Shin YS, Kim SM, Kim YU, Kim YK, Kim SY, Kim YJ, Cho MK, Lee GJ
- KMID: 2274999
- Chonnam Med J.
- 2001 Sep;37(3):299-303.
Patients with Gitelman's syndrome present a variety of clinical features, such as hypokalemia, hypomagnesemia, hypocalciuria and metabolic alkalosis, mostly in their adulthood or adolescence. Their ability to concentrate urine is... -
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- Clinical Study of a Newly Diagnosed Case of Gitelman Syndrome in a Patient Monitored for Liddle Syndrome
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Park JH, Kim HY, Kim DH, Kim JW, Kim SH, Park WD
- KMID: 2387007
- Soonchunhyang Med Sci.
- 2016 Dec;22(2):136-140.
- doi: 10.0000/sms.2016.22.2.136
A 55-year-old man who had been monitored for Liddle syndrome in the nephrology division for 15 years visited again Inje University Sanggye Paik Hospital for a newly developed electrolyte disorder.... -
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- A case of Gitelman's Syndrome with Chronic Hypotension and Normomagnesemia
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Jun HJ, Cho SK, Choi SB, Seo JS, Kang SW, Kim YH, Kang MS, Kim WY, Kim J, Kim YW
- KMID: 2079752
- Korean J Nephrol.
- 2007 Jul;26(4):460-464.
Gitelman's syndrome is a heritable renal disorder characterized by hypomagnesemia, hypokalemia and hypocalciuria. Interestingly, we have experienced one patient who had chronic hypotension, normal serum magnesium level, normal plasma ionized... -
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- A Case of Gitelman Syndrome Presented with Epileptic Seizure
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Park JM, Kim JT, Shin JI, Kim HD, Kim TY, Cheong HI, Lee JS
- KMID: 2197657
- J Korean Soc Pediatr Nephrol.
- 2004 Apr;8(1):68-73.
Both Gitelman syndrome and Bartter syndrome are autosomal recessively inherited renal tubular disorders characterized by hypokalemic metabolic alkalosis, salt wasting and normal to low blood pressure. Gitelman syndrome is caused... -
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- Rheumatoid arthritis accompanied by Gitelman syndrome
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Park MG, Lee JH, Kim SJ, Park SH, Park SK, Choi JS, Hwang JY
- KMID: 2400338
- Yeungnam Univ J Med.
- 2017 Jun;34(1):101-105.
- doi: 10.12701/yujm.2017.34.1.101
Gitelman syndrome is a condition caused by a mutation of the thiazide sensitive Na-Cl cotransporter gene on the distal convoluted tubule. It results in a variety of clinical features, including... -
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- Disorders of Electrolyte Metabolism, Bartter Syndrome and Gitelman Syndrome
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Kim K, Kim KH, Kim PK
- KMID: 1517050
- Korean J Pediatr.
- 2004 Dec;47(Suppl 4):S772-S784.
No abstract available. -
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- Two Cases of Gitelman's Syndrome Diagnosed by Renal Clearance Study
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Kim TH, Kim SJ, Seo YK, Shim JY, Jung HL, Park MS, Kum DH
- KMID: 2335609
- J Korean Pediatr Soc.
- 2002 Mar;45(3):413-417.
Gitelman's syndrome is an autosomal recessive disorder characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria that has recently been reported to be linked to thiazide-sensitive Na-Cl cotransporter gene mutation. In... -
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- Gitelman Syndrome with Normal Serum Magnesium
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Cheon Y, Seo JH, Cheong HI, Park YH
- KMID: 2322036
- J Korean Soc Pediatr Nephrol.
- 2012 Oct;16(2):121-125.
Gitelman syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemic metabolic alkalosis, and it is distinguished from Batter syndrome by hypomagnesemia and hypocalciuria. This disorder is caused by... -
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- A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome
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Cho HW, Lee ST, Cho H, Cheong HI
- KMID: 2362268
- Korean J Pediatr.
- 2016 Nov;59(Suppl 1):S103-S106.
- doi: 10.3345/kjp.2016.59.11.S103
Bartter syndrome (BS) is an inherited renal tubular disorder characterized by low or normal blood pressure, hypokalemic metabolic alkalosis, and hyperreninemic hyperaldosteronism. Type III BS is caused by loss-of-function mutations... -
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- Wilson Disease Comorbid with Hereditary Sensory Autonomic Neuropathy Type IV and Gitelman Syndrome
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Kim JY, Park SS, Yang HR
- KMID: 2451580
- Pediatr Gastroenterol Hepatol Nutr.
- 2019 Jul;22(4):392-399.
- doi: 10.5223/pghn.2019.22.4.392
Wilson disease a rare autosomal recessive inherited disorder of copper metabolism, is characterized by excessive deposition of copper in the liver, brain, and other tissues. Wilson disease is often fatal... -
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- Absence of intact thiazide-sensitive sodium-chloride cotransporter in the renal tissue of a Gitelman's syndrome patient
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Jang HR, Heo NJ, Son MJ, Lee JW, Lee JH, Jeon US, Shin SJ, Na KY, Joo KW, Lee JS, Cheong HI, Kim J, Han JS
- KMID: 2081172
- Korean J Med.
- 2005 Dec;69(6):642-650.
BACKGROUND: Gitelman's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. It is known to be caused by a mutation of SLC12A3 gene... -
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