Acquired Gitelman Syndrome [PDF]
Electrolytes & Blood Pressure, 2009 Acquired renal tubular disorder can be observed in various disease processes, especially autoimmune diseases. Gitelman syndrome is an autosomal recessive disease characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria.
Kim, Yong Kyun +3 more
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Gitelman Syndrome in a Case of Diabetic Kidney Disease: A Diagnostic and Therapeutic Dilemma [PDF]
Journal of Clinical and Diagnostic Research, 2018 Gitelman syndrome is an autosomal recessive disorder that usually presents with hypokalemia, hypomagnesemia, hypocalciuria and normal blood pressure. In contrast to Bartter syndrome it presents in late adulthood.
Vaibhav Seth +4 more
doaj +1 more source
A Case of Gitelman Syndrome with Hypercalcemia Secondary to Primary Hyperparathyroidism
Case Reports in Endocrinology, 2022 Gitelman syndrome is a rare autosomal recessive salt-losing tubulopathy characterized by hypokalemia, hypomagnesemia, hypocalciuria, and secondary hyperaldosteronism. However, hypercalcemia secondary to hypocalciuria is extremely rare during the disease.
Zeinab Alnahas +2 more
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Quadriparesis due to Gitelman′s syndrome diagnosed with thiazide diuretic test response
Saudi Journal of Kidney Diseases and Transplantation, 2016 Gitelman′s syndrome is characterized by hypocalciuria, severe hypomagnesemia, and prominent muscular involvements such as fatigue, weakness, cramps, and tetany. It is due to mutations in the thiazide sensitive NaCl co-transporter in the distal convoluted
Sumanto Mukhopadhyay +5 more
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Central Executive Dysfunction and Deferred Prefrontal Processing in Veterans with Gulf War Illness. [PDF]
, 2013 Gulf War Illness is associated with toxic exposure to cholinergic disruptive chemicals. The cholinergic system has been shown to mediate the central executive of working memory (WM).
Bennett, Ilana J +7 more
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Anaesthesia for emergency caesarean section in a patient with Gitelman syndrome
Indian Journal of Anaesthesia, 2020 Gitelman syndrome is a rare autosomal recessive salt-losing disorder of renal tubules, which results in hypokalemic metabolic alkalosis. Associated hypomagnesaemia and hypocalcaemia are also seen.
Sarath Venugopalan +3 more
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Mutationsanalysen bei hereditären Salzverlusttubulopathien [PDF]
, 2004 Der Begriff Bartter-Syndrom stellt den historisch bedingten Sammelbegriff für einige hereditäre Tubulopathien dar, denen eine chronische hypokaliämische metabolische Alkalose gemein ist.
Ott, Henning +1 more
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Anesthetic management of child with Gitelman Syndrome: case report
Brazilian Journal of Anesthesiology, 2021 Gitelman syndrome is a rare autosomal recessive inherited disease that affects the thiazidesensitive sodium-chloride cotransport channels and the magnesium channels in the distal convoluted tubule, leading to hypokalemic metabolic alkalosis ...
Sara Ferreira +3 more
doaj +1 more source
Magnesium lactate in the treatment of Gitelman syndrome: patient-reported outcomes. [PDF]
, 1997 BACKGROUND: Gitelman syndrome (GS) is a rare recessively inherited renal tubulopathy associated with renal potassium (K) and magnesium (Mg) loss. It requires lifelong K and Mg supplementation at high doses that are at best unpalatable and at worst ...
A. Ingsathit +40 more
core +33 more sources
Gitelman′s syndrome with panhypopituitarism: Reno-endocrine interplay
Indian Journal of Endocrinology and Metabolism, 2012 Gitelman′s syndrome is an inherited tubulopathy affecting thiazide-sensitive sodium chloride cotransporter, which manifests with hypokalemic alkalosis, hypomagnesemia, and hypocalciuria.
Vimal Upreti +4 more
doaj +1 more source