Abstract | OBJECTIVE: Familial occurrence of Bartter's syndrome is well known, but the simultaneous occurrence of hypokalemia/hypomagnesemia and chondrocalcinosis in one family has not been described. We present the clinical, laboratory and radiological findings of a family, in which 7 members were affected by disease. METHODS: A total of 43 members of the family could be interviewed concerning their general health, past diseases and joint complaints. Serum potassium and magnesium were determined in all and radiographic studies were performed in those who had hypokalemia and hypomagnesemia or those with merely articular complaints. Urinary excretion of potassium, magnesium and calcium were determined in the affected persons. RESULTS: Seven patients were found with hypokalemia and hypomagnesemia. Urinary potassium and magnesium excretion was inappropriately high when compared to the serum levels of these electrolytes. All patients had hypocalciuria and extensive chondrocalcinosis, mainly in the knees, elbows and shoulders. In one patient, most probably as a result of magnesium supplementation, a striking reduction of chondrocalcinosis was observed during a followup of 10 years. CONCLUSION:
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Authors | T J Smilde, J F Haverman, P Schipper, A R Hermus, F J van Liebergen, J L Jansen, P W Kloppenborg, M I Koolen |
Journal | The Journal of rheumatology
(J Rheumatol)
Vol. 21
Issue 8
Pg. 1515-9
(Aug 1994)
ISSN: 0315-162X [Print] Canada |
PMID | 7983657
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Electrolytes
- Magnesium
- Potassium
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Topics |
- Adult
- Bartter Syndrome
(blood, diagnostic imaging, genetics, urine)
- Chondrocalcinosis
(blood, diagnostic imaging, genetics, urine)
- Electrolytes
(blood)
- Female
- Follow-Up Studies
- Humans
- Hypokalemia
(blood, genetics, urine)
- Magnesium
(blood, urine)
- Male
- Middle Aged
- Pedigree
- Potassium
(urine)
- Radiography
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