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Gitelman syndrome (GS) is an autosomal recessive, salt-losing tubulopathy characterized by renal potassium wasting, hypokalemia, metabolic alkalosis, hypocalciuria, hypomagnesemia, and hyperreninemic hyperaldosteronism. [1] Gitelman syndrome is also referred to as familial hypokalemia-hypomagnesemia.
May 16, 2023
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Feb 1, 2011 · Gitelman syndrome is a kidney disorder that causes an imbalance of charged atoms (ions) in the body, including ions of potassium, magnesium, ...
Gitelman syndrome, also known as familial hypokalemia-hypomagnesemia, is a rare genetic disorder in which there is a specific defect in kidney function. This ...
Gitelman syndrome (GS) is an autosomal recessive kidney tubule disorder characterized by low blood levels of potassium and magnesium, decreased excretion of ...

Gitelman syndrome

Disorder
Gitelman syndrome is an autosomal recessive kidney tubule disorder characterized by low blood levels of potassium and magnesium, decreased excretion of calcium in the urine, and elevated blood pH. It is the most frequent hereditary salt-losing... Wikipedia
Jul 30, 2008 · Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by hypokalemic metabolic alkalosis in ...
Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria.
A rare syndrome characterized by hypokalemic metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion. ORPHA:358.
Gitelman syndrome, also known as familial hypokalemia hypomagnesemia, is an inherited autosomal recessive kidney disorder that impacts the reabsorption of ...
Mar 7, 2023 · RELATED TOPICS · Bartter and Gitelman syndromes in children: Clinical manifestations, diagnosis, and management · Cisplatin nephrotoxicity ...
Oct 2, 2019 · Gitelman syndrome is an inherited tubulopathy characterized by renal salt wasting from the distal convoluted tubule. Defects in the sodium ...