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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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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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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
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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
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Gitelman syndrome associated with chondrocalcinosis: description of two cases
Reumatismo, 2011 Gitelman syndrome is a rare inherited tubulopathy, characterized by hypomagnesemia, hypokalemia, metabolic alkalosis, hypocalciuria and hyperreninemic hyperaldosteronism.
E. Filippucci +7 more
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Comorbid Gitelman Syndrome and Schizophrenia: A Case Report [PDF]
Düşünen Adam Psikiyatri ve Nörolojik Bilimler Dergisi, 2006 In this report, a 28 year old schizophrenic patient who had Gitelman syndrome comorbidity is presented and the differential diagnosis is discussed. Gitelman syndrome is, defined as an autosomal recessive disorder featuring hypokalemic metabolic alkalosis,
Huriye Gümüş +2 more
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Sri Lanka Journal of Diabetes Endocrinology and Metabolism, 2020 Background Hypokalaemic paralysis is a rare group of disorders with concomitant muscle weakness and hypokalaemia. Thyrotoxicosis is a recognized and a common cause for hypokalaemic paralysis among Asians, in which intracellular shift of potassium is ...
Chandrika Jayakanthi subasinghe +6 more
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A Case of Gitelman Syndrome; Incidentally Diagnosed in Elderly
Bezmiâlem Science, 2022 Gitelman syndrome is an autosomal recessive renal tubular disease that is followed by symptoms, such as fatigue, muscle weakness, tetany, polydipsia, and nocturia.
Selma KARAAHMETOĞLU +1 more
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HELLP syndrome in a pregnant patient with Gitelman syndrome
Kidney Research and Clinical Practice, 2017 Gitelman syndrome is characterized by hypokalemia, metabolic alkalosis, hypocalciuria, and hypomagnesemia. The clinical course of Gitelman syndrome in pregnant women remains unclear, but it is thought to be benign. We report here the first Korean case of
Minhyeok Lee +7 more
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Jurnal Kesehatan Andalas. 2019; 8(4) Gitelman Syndrome
Jurnal Kesehatan Andalas, 2020 Abstrak Gitelman syndrome (GS) adalah gangguan tubular ginjal bersifat autosom resesif yang ditandai dengan hipokalemia, alkalosis metabolik, hipomagnesemia dan hipokalsiuria.
Venni Dimitri, Drajat Priyono
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