Familial Bartter's syndrome.
Toshio Ogihara, Anna Maruyama, Charles A. Nugent, Takeshi Hata, Hiroshi Mikami, Y Kumahara
Abstract
Toshio Ogihara, Anna Maruyama, Charles A. Nugent, Takeshi Hata, Hiroshi Mikami, Y Kumahara
Abstract
Two sisters were found to have Bartter's syndrome. Both had hypokalemia, hyperreninemia, normal BPs, and decreased pressor responses to angiotensin II. During a water diuresis, patient 1 had an abnormally low distal tubular fractional reabsorption of chloride initially, but this normalized after hypokalemia was corrected for one year. Patient 2 had no demonstrable defect in chloride transport. Hypokalemia in Bartter's syndrome may be caused by some hereditary mechanisms other than defective reabsorption of chloride in the distal tubules.
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Two sisters were found to have Bartter's syndrome. Both had hypokalemia, hyperreninemia, normal BPs, and decreased pressor responses to angiotensin II. During a water diuresis, patient 1 had an abnormally low distal tubular fractional reabsorption of chloride initially, but this normalized after hypokalemia was corrected for one year. Patient 2 had no demonstrable defect in chloride transport. Hypokalemia in Bartter's syndrome may be caused by some hereditary mechanisms other than defective reabsorption of chloride in the distal tubules.
Key concepts: Hypokalemia, Bartter's syndrome, Reabsorption, Endocrinology, Bartter syndrome, Internal medicine, Diuresis, Chemistry