A 28-year-old female patient was hospitalized for mild–moderate hypokalaemia which was persistent despite discontinuation of beta-2 agonist bronchodilator treatment. Her past medical history was relevant for two episodes of severe hypokalaemia after active inhaled beta-2 agonist treatment for asthma crisis. Investigations revealed increased potassium in spot urine with a transtubular potassium gradient <4. A 24-hour urine analysis showed hypophosphaturia, hypocalciuria, hypomagnesuria and normal urine prostaglandins in favour of Gitelman syndrome. Oral potassium supplementation was started and genetic studies were recommended
Gitelman’s syndrome is a primary renal tubular disorder resulting from a defective absorption of sod...
The authors present an introduction to hypokalemia and then discuss a case report on a patient with ...
Hypokalemia and metabolic alkalosis can be present in different rare diseases, and the differential ...
Hypokalaemia is a common clinical disorder, the cause of which can usually be determined by the pati...
Introduction: Hypokalemia is common disorder characterized by low plasma potassium levels (<3.5 m...
Potassium is critical for many important cell functions. Hereditary tubulopathies can also present i...
Abstract The main causes of hypokalemia are usually evident in the clinical history of patients, wit...
Objective: We present an uncommon case of surreptitious diuretic usage mimicking Gitelman syndrome. ...
AbstractIntroductionHypokalaemia is a common clinical problem. A potential but commonly overlooked c...
Gitelman syndrome is a rare renal tubule disease characterized by hypokalaemia, metabolic alkalosis,...
Gitelman syndrome (GS) is a rare renal disorder, and little is known about its impact on pregnancy. ...
Gitelman syndrome is a salt-wasting tubulopathy characterized by profound hypokalemia, hypomagnesemi...
Gitelman syndrome(GS) is a rare autosomal recessive salt-losing tubulopathy of young adults, charact...
Gitelman syndrome is a rare, inherited disorder. Hypokalemia, meta-bolic alkalosis, hypomagnesemia a...
The Gitelman and Bartter syndromes (GS and BS, respectively) are characterized by the constellation ...
Gitelman’s syndrome is a primary renal tubular disorder resulting from a defective absorption of sod...
The authors present an introduction to hypokalemia and then discuss a case report on a patient with ...
Hypokalemia and metabolic alkalosis can be present in different rare diseases, and the differential ...
Hypokalaemia is a common clinical disorder, the cause of which can usually be determined by the pati...
Introduction: Hypokalemia is common disorder characterized by low plasma potassium levels (<3.5 m...
Potassium is critical for many important cell functions. Hereditary tubulopathies can also present i...
Abstract The main causes of hypokalemia are usually evident in the clinical history of patients, wit...
Objective: We present an uncommon case of surreptitious diuretic usage mimicking Gitelman syndrome. ...
AbstractIntroductionHypokalaemia is a common clinical problem. A potential but commonly overlooked c...
Gitelman syndrome is a rare renal tubule disease characterized by hypokalaemia, metabolic alkalosis,...
Gitelman syndrome (GS) is a rare renal disorder, and little is known about its impact on pregnancy. ...
Gitelman syndrome is a salt-wasting tubulopathy characterized by profound hypokalemia, hypomagnesemi...
Gitelman syndrome(GS) is a rare autosomal recessive salt-losing tubulopathy of young adults, charact...
Gitelman syndrome is a rare, inherited disorder. Hypokalemia, meta-bolic alkalosis, hypomagnesemia a...
The Gitelman and Bartter syndromes (GS and BS, respectively) are characterized by the constellation ...
Gitelman’s syndrome is a primary renal tubular disorder resulting from a defective absorption of sod...
The authors present an introduction to hypokalemia and then discuss a case report on a patient with ...
Hypokalemia and metabolic alkalosis can be present in different rare diseases, and the differential ...