1.A Case of Bartter'S Syndrome.
Yung Suk SONG ; Moon Ho CHUNG ; Ha Baik LEE ; Chong Moo PARK
Journal of the Korean Pediatric Society 1983;26(6):611-615
No abstract available.
Bartter Syndrome*
2.A Case of Bartter's Syndrome.
Jeong A HWANG ; Jung Hye CHOI ; Jae Seung LEE
Journal of the Korean Pediatric Society 1987;30(8):922-927
No abstract available.
Bartter Syndrome*
3.A case of Bartter's syndrome.
Ho Young PYUN ; Sung Bae PARK ; Hee Young CHO ; Kyung Min LEE
Korean Journal of Nephrology 1992;11(1):78-84
No abstract available.
Bartter Syndrome*
4.A case of Bartter's syndrome.
Kyu Young LEE ; Byoung Soo CHO ; Hah Young LEE ; Jay BERNSTEIN
Journal of the Korean Pediatric Society 1991;34(6):849-856
No abstract available.
Bartter Syndrome*
;
Indomethacin
5.Disorders of Electrolyte Metabolism, Bartter Syndrome and Gitelman Syndrome.
KyoSun KIM ; Kee Hyuck KIM ; Pyung kil KIM
Korean Journal of Pediatrics 2004;47(Suppl 4):S772-S784
No abstract available.
Bartter Syndrome*
;
Gitelman Syndrome*
;
Metabolism*
6.A Case of Atypical Gitelman's Syndrome with Normomagnesemia and Normal Magnesium Excretion.
Jin Seok JEON ; Young Min KIM ; Hyunjin NOH ; Dong Cheol HAN
Korean Journal of Nephrology 2004;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 features of Gitelman's syndrome. Interestingly, we have experienced a case of 32-year old man with a mixed type of Gitelman's syndrome and Bartter's syndrome, which includes normomagnesemia, normal renal magnesium excretion, and hypocalciuria. Herein we report the case of atypical Gitelman's syndrome with brief review of related literature.
Adult
;
Bartter Syndrome
;
Calcium
;
Gitelman Syndrome*
;
Humans
;
Hypokalemia
;
Magnesium*
7.Two cases with Bartter syndrome who had diarrhea as symptom of onset.
Chinese Journal of Pediatrics 2003;41(7):557-557
Bartter Syndrome
;
complications
;
Diarrhea
;
etiology
;
Female
;
Humans
;
Infant
;
Male
;
Syndrome
9.Renal potassium wasting and hypocalciuria ameliorated with magnesium repletion in Gitelman's syndrome.
Young Jung CHO ; Geun Tae PARK ; Yun Ju CHO ; Ho Jung KIM
Journal of Korean Medical Science 1997;12(2):157-159
A woman aged 45 years was presented with hypokalemic metabolic alkalosis and hypomagnesemia associated with renal potassium and magnesium wasting. Her 24-hour urinary calcium excretion was strikingly low despite normocalcemia and normal creatinine clearance, which is one of characteristic findings of Gitelman's syndrome (GS). She was evaluated for the responses following Mg supplementation for 10 days, which showed marked increments in serum potassium and magnesium as well as improvements of the degree of renal potassium wasting and hypocalciuria. This amelioration of abnormal biochemical pictures in this patient after Mg supplementation proposes that the hypokalemia with renal potassium wasting and hypocalciuria may be caused by abnormal Mg metabolism.
Bartter's Disease/urine
;
Bartter's Disease/therapy*
;
Bartter's Disease/blood
;
Calcium/urine*
;
Case Report
;
Female
;
Food, Fortified
;
Human
;
Hypokalemia/therapy*
;
Magnesium/blood*
;
Middle Age
;
Syndrome
10.A Case of Gitelman Syndrome Presented with Epileptic Seizure.
Jee Min PARK ; Jeong Tae KIM ; Jae Il SHIN ; Heung Dong KIM ; Tae Young KIM ; Hae Il CHEONG ; Jae Seung LEE
Journal of the Korean Society of Pediatric Nephrology 2004;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 by mutations in the thiazide-sensitive Na- Cl cotransporter (NCCT) and distinguished from Bartter syndrome, which is associated with mutations of several genes, by the presence of hypomagnesemia and hypocalciuria. In most of the patients with Gitelman syndrome, the disease manifests with transient episodes of muscular weakness and tetany in the adult period, but, often, is asymptomatic. We report here an 11 years-old female with Gitelman syndrome who presented with aggravation of epileptic seizure. The diagnostic work-up showed typical clinical features of metabolic alkalosis, hypokalemia, hypomagnesemia and hypocalciuria. We also identified a heterozygote mutation(642CGC(Arg)>TGC(Cys)) and an abnormal splicing in the SLC12A3 gene encoding NCCT.
Adult
;
Alkalosis
;
Bartter Syndrome
;
Child
;
Epilepsy*
;
Female
;
Gitelman Syndrome*
;
Heterozygote
;
Humans
;
Hypokalemia
;
Hypotension
;
Muscle Weakness
;
Tetany