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10.1097/MD.0000000000016408 http://scihub22266oqcxt.onion/10.1097/MD.0000000000016408 31305454!6641743!31305454     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=31305454&cmd=llinks): Failed to open stream: HTTP request failed! 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Gitelman s syndrome with hyperphosphatemia, effectively responding to single oral magnesium oxide administration: A case report |pdf=|usr=}}{{31305454}} gab.com Text Gitelman s syndrome with hyperphosphatemia, effectively responding to single oral magnesium oxide administration: A case report JO: Medicine (Baltimore) http://www.kidney.de/pget.php?&tw=1&pmid=31305454 #FOAvip RATIONALE: The Gitelman's syndrome (GS) is characterized by metabolic alkalosis, hypokalemia, hypomagnesemia, and hypocalciuria. However, the involvement of this deranged electrolyte balance in patients with GS in parathyroid hormone action has not been known. PATIENT CONCERNS: We report a 34-year-old woman with muscle weakness and tetany/seizures caused by electrolyte imbalance. She had hyperphosphatemia and hypocalciuric hypocalcemia in addition to severe hypomagnesemia with low potassium in the absence of metabolic alkalosis. We identified 2 heterozygous mutations in the solute carrier family 12 member 3 gene in this case (c.1732G>A, p.Val578Met and c.2537_38delTT, p.846fs) by targeted sequence for all causative genes of salt-losing tubulopathies. DIAGNOSES: A diagnosis of GS. Hypocalcemia and hyperphosphatemia were suggested to relate with the secondary obstruction of appropriate parathyroid hormone release following severe hypomagnesemia in GS. INTERVENTIONS: She was treated with single oral magnesium oxide administration. OUTCOMES: The electrolyte imbalance including hypocalcemia and hyperphosphatemia were resolved with a remission of clinical manifestations. LESSONS: These observations, in this case, suggest that even severe hypomagnesemia caused by GS was associated with resistance to appropriate parathyroid hormone secretion. Through this case, we recognize that secondary hypoparathyroidism would be triggered by severe hypomagnesemia in GS. Twit Text FOAVip Gitelman s syndrome with hyperphosphatemia, effectively responding to single oral magnesium oxide administration: A case report ????Medicine (Baltimore) http://www.kidney.de/pget.php?&tw=1&pmid=31305454 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=31305454 #FOAvip English Wikipedia <ref>{{Cite pmid|31305454}}</ref> Gitelman s syndrome with hyperphosphatemia, effectively responding to single oral magnesium oxide administration: A case report #MMPMID31305454 Miya A; Nakamura A; Kameda H; Nozu K; Miyoshi H; Atsumi T Medicine (Baltimore) 2019[Jul]; 98 (28): e16408 PMID31305454show ga RATIONALE: The Gitelman's syndrome (GS) is characterized by metabolic alkalosis, hypokalemia, hypomagnesemia, and hypocalciuria. However, the involvement of this deranged electrolyte balance in patients with GS in parathyroid hormone action has not been known. PATIENT CONCERNS: We report a 34-year-old woman with muscle weakness and tetany/seizures caused by electrolyte imbalance. She had hyperphosphatemia and hypocalciuric hypocalcemia in addition to severe hypomagnesemia with low potassium in the absence of metabolic alkalosis. We identified 2 heterozygous mutations in the solute carrier family 12 member 3 gene in this case (c.1732G>A, p.Val578Met and c.2537_38delTT, p.846fs) by targeted sequence for all causative genes of salt-losing tubulopathies. DIAGNOSES: A diagnosis of GS. Hypocalcemia and hyperphosphatemia were suggested to relate with the secondary obstruction of appropriate parathyroid hormone release following severe hypomagnesemia in GS. INTERVENTIONS: She was treated with single oral magnesium oxide administration. OUTCOMES: The electrolyte imbalance including hypocalcemia and hyperphosphatemia were resolved with a remission of clinical manifestations. LESSONS: These observations, in this case, suggest that even severe hypomagnesemia caused by GS was associated with resistance to appropriate parathyroid hormone secretion. Through this case, we recognize that secondary hypoparathyroidism would be triggered by severe hypomagnesemia in GS. |Administration, Oral[MESH] |Adult[MESH] |Antacids/*therapeutic use[MESH] |Female[MESH] |Gitelman Syndrome/*complications/*drug therapy/genetics[MESH] |Humans[MESH] |Hyperphosphatemia/*complications/*drug therapy/genetics[MESH]Gitelman s syndrome with hyperphosphatemia, effectively responding to (epmc).pdf DeepDyve Pubget Overpricing