- A case of Bartter's syndrome
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Lee KY, Cho BS, Lee HY, Bernstein
- KMID: 1691779
- J Korean Pediatr Soc.
- 1991 Jun;34(6):849-856.
No abstract available. -
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- A case of Bartter's syndrome
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Yoon JH, Kwon JE, Lee JO, Lee SG
- KMID: 1945912
- J Korean Pediatr Soc.
- 1993 Sep;36(9):1308-1314.
Bartter's syndrome is a rare tubular disorder characterized by hypokalemic, hypochloremic metabolic alkalosis, hyperreninemic hyperaldosteronism, hyporesponsiveness to pressor agents, and juxtaglomerular apparatus hyperplasia. We report here a case of Bartter's... -
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- A Case of Adult-Onset Bartter's Syndrome Associated with Nephrocalcinosis
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Oh HJ, Rim H, Jung YS
- KMID: 2079692
- Korean J Nephrol.
- 2007 May;26(3):353-357.
Bartter syndrome is characterized by markedly reduced or absent salt transport by the thick ascending limb of Henle. The phenotype of Bartter syndrome is renal salt wasting, hypokalemic metabolic alkalosis,... -
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- A Case of Bartter's Syndrome
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Hwang JA, Choi JH, Lee JS
- KMID: 1677087
- J Korean Pediatr Soc.
- 1987 Aug;30(8):922-927.
No abstract available. -
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- A Case of Adult onset Bartter Syndrome with Nephrocalcinosis
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Park MG, Lim TW, Oh HT, Song SU, Heo D, Rim H
- KMID: 1882443
- Kosin Med J.
- 2014 Jun;29(1):75-79.
- doi: 10.7180/kmj.2014.29.1.75
Bartter syndrome is a renal tubular defect in electrolyte transport characterized by hypokalemia, metabolic alkalosis, hyperreninemia, hyperaldosteronism, normal blood pressure, and other clinical symptoms. As a clinical and genetical heterogeneous disorder,... -
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- A Case of Bartter'S Syndrome
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Song YS, Chung MH, Lee HB, Park CM
- KMID: 1699160
- J Korean Pediatr Soc.
- 1983 Jun;26(6):611-615.
No abstract available. -
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- A case of Bartter's syndrome
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Pyun HY, Park SB, Cho HY, Lee KM
- KMID: 1694808
- Korean J Nephrol.
- 1992 Mar;11(1):78-84.
No abstract available. -
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- A Case of Bartter's Syndrome with a Seizure Disorder Associated with Subdural Hematoma
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Lee JJ, Moon HK, Park YH
- KMID: 2352255
- Yeungnam Univ J Med.
- 1994 Dec;11(2):388-397.
- doi: 10.12701/yujm.1994.11.2.388
Bartter's syndrome is a rare tubular disorder characterized by hypokalemic, hypochloremic metabolic alkalosis, hyperreninemic, hyperaldosteronism, hyporesponsiveness to pressor agents and juxtaglomerular apparatus heperplasia. We report a case of Bartter's syndrome of... -
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- A Case of Bartter Syndrome with Muscle Weakness and Short Stature
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Kim IS, Kang JH, Shin YH, Lee DK, Kim SN, Pai KS
- KMID: 2322078
- J Korean Soc Pediatr Nephrol.
- 2002 Oct;6(2):259-265.
Bartter syndrome is a rare disorder characterized by the association of hypokalemic hypochloremic metabolic alkalosis, hyperreninemia, hyperaldosteronemia, short stature and nephrocalcinosis. This disorder presents with hyperplasia of juxtaglomerular apparatus on... -
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- Furosemide induced medullary nephrocalcinosis mimicking Bartter syndrome
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Kim S, Kyung C, Kim YH, Cho JH, Hwang C, Lee JE
- KMID: 2319925
- Yeungnam Univ J Med.
- 2014 Jun;31(1):21-24.
Clinical presentation of Bartter syndrome is similar to surrepitious vomiting or use of diuretics. Therefore, precise differential diagnosis of Bartter syndrome is crucial. We report a case of medullary nephrocalcinosis... -
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- A Case of Pseudo-Bartter's Syndrome Due to Hypertrophic Pyloric Stenosis
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Kim YH, Lee TH, Kim HB
- KMID: 2335698
- J Korean Pediatr Soc.
- 2002 Nov;45(11):1430-1434.
We report a 3-month old boy admitted to our hospital with Bartter's syndrome like symptoms and laboratory findings, which were vomiting, failure to thrive, hypochloremic and hypokalemic metabolic alkalosis associated... -
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- 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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- A Case of Neonatal Bartter Syndrome
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Ryu JM, Lee JH, Han HW, Park YS
- KMID: 1627752
- J Korean Soc Pediatr Nephrol.
- 2005 Oct;9(2):255-262.
Bartter and Bartter-like syndromes, which include classic Bartter syndrome(type III), neonatal Bartter syndrome(type I, II or IV) and Gitelman syndrome, are autosomal - recessively inherited renal tubular disorders characterized by... -
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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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- 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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- A Case of Bartter-like Syndrome in a Patient of Drug-induced Interstitial Nephritis Associated with Rheumatoid Arthritis
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Park YI, Park YH, Kim SO, Lee KI, Kwak LS, Na HY
- KMID: 2254766
- Korean J Nephrol.
- 1997 Dec;16(4):778-782.
A 59-year-old female patient with rheumatoid arthritis showed hypokalemic metabolic alkalosis, normotensive hyperreninemic hyperaldosteronism and high urinary prostaglandin level. She was thought to have Bartter's syndrome. But, her kidney biopsy... -
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- A case of Bartter's syndrome in adult female patient
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Che DH, Yang SH, Park BC, Jung YH, Lee K, Yang YP, Kim HJ, Jo JK, Byun JH, Park MH
- KMID: 1698171
- Korean J Intern Med.
- 1992 Jul;43(1):112-118.
No abstract available. -
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- A case of Bartter's syndrome in an adult
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Lee HY, Chung YS, Ahn KJ, Lee SW, Kim MR, Kim YK, Choi KH, Lee HC, Han DS, Huh KB, Kim KH, Jung HJ
- KMID: 1697919
- Korean J Intern Med.
- 1991 Jun;40(6):844-852.
No abstract available. -
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- A Case of Bartter's Syndrome in an Adult
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Song JS, Shinn JJ, You KH, Lee HK, Cha WK, Kwon KH, So YS, Kim JS, Cho JT
- KMID: 2307395
- Korean J Nephrol.
- 1997 Sep;16(3):567-571.
Bartter's syndrome is characterized by hypokalemia and secondary hyperaldosteronism without edema or hypertension. Its pathogenesis is obscure and the characteristic renal potassium wastage is difficult to treat. We experienced a... -
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- Autosomal dominant hypocalcemia with Bartter syndrome due to a novel activating mutation of calcium sensing receptor, Y829C
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Choi KH, Shin CH, Yang SW, Cheong HI
- KMID: 1802615
- Korean J Pediatr.
- 2015 Apr;58(4):148-153.
- doi: 10.3345/kjp.2015.58.4.148
The calcium sensing receptor (CaSR) plays an important role in calcium homeostasis. Activating mutations of CaSR cause autosomal dominant hypocalcemia by affecting parathyroid hormone secretion in parathyroid gland and calcium... -
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