A 26-year-old female with Bartter's syndrome associated with Graves' disease is reported. This patient had a history of Graves' disease from the age of 22 and anti-thyroid drug (Methimazole) had been administered for 2 years. Thyroid function returned to normal but general fatigue and polyuria continued. Hypokalemia was diagnosed at 25 years of age and she was referred to our hospital for evaluation. Blood pressure was normal and laboratory data revealed normal thyroid function, hypokalemic alkalosis, high plasma renin activity and high plasma aldosterone concentration. She showed normal pressor sensitivity to norepinephrine infusion, grossly diminished pressor sensitivity to exogenous angiotensin II infusion compared with the normal. A ren...
We report a case of a woman who came to our attention because of hypokalemia, hyperreninemia and hyp...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
A case of familial Bartter's syndrome is reported. The child had early and severe clinical and bioch...
A 26-year-old female with Bartter's syndrome associated with Graves' disease is reported. This patie...
We describe an unusual clinical presentation of autoimmune Bartter syndrome in a patient with primar...
Bartter's syndrome is characterized by hypokalemia, metabolic alkalosis, hyperreninemia and seconda...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
Bartter's syndrome with hyperplasia of renomedullary cells: Successful treatment with indomethacin. ...
We report a rare case of Bartter's syndrome in a 35-year-old woman with type 2 diabetes mellitus. Th...
Three and half year old Haleema presented to OPD with complaints of failure to thrive polydipsia and...
Abstract Background Bartter’s syndrome is a rare genetic tubulopathy affecting the loop of Henle lea...
Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male pa...
Bartter syndrome is a rare inherited disorder which usually presents in childhood and is characteriz...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
We report a rare case of Bartter’s syndrome in a 35-year-old woman with type 2 diabetes mellitus. Th...
We report a case of a woman who came to our attention because of hypokalemia, hyperreninemia and hyp...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
A case of familial Bartter's syndrome is reported. The child had early and severe clinical and bioch...
A 26-year-old female with Bartter's syndrome associated with Graves' disease is reported. This patie...
We describe an unusual clinical presentation of autoimmune Bartter syndrome in a patient with primar...
Bartter's syndrome is characterized by hypokalemia, metabolic alkalosis, hyperreninemia and seconda...
Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivatio...
Bartter's syndrome with hyperplasia of renomedullary cells: Successful treatment with indomethacin. ...
We report a rare case of Bartter's syndrome in a 35-year-old woman with type 2 diabetes mellitus. Th...
Three and half year old Haleema presented to OPD with complaints of failure to thrive polydipsia and...
Abstract Background Bartter’s syndrome is a rare genetic tubulopathy affecting the loop of Henle lea...
Bartter's syndrome is a rare inherited renal tubular disorder. We experienced an 8-month old male pa...
Bartter syndrome is a rare inherited disorder which usually presents in childhood and is characteriz...
Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochlo...
We report a rare case of Bartter’s syndrome in a 35-year-old woman with type 2 diabetes mellitus. Th...
We report a case of a woman who came to our attention because of hypokalemia, hyperreninemia and hyp...
Bartter syndrome comprises a group of rare autosomal-recessive salt-losing disorders with distinct p...
A case of familial Bartter's syndrome is reported. The child had early and severe clinical and bioch...