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A Case of Isolated Glycosuria Mediated by an SLC5A2 Gene Mutation and Characterized by Postprandial Heavy Glycosuria Without Salt Wasting

Kim KM, Kwon SK, Kim HY

Familial renal glycosuria (FRG) is an inherited disorder characterized by persistent glycosuria in the absence of hyperglycemia. It is caused by mutations in the sodium-glucose co-transporter, leading to increase in...
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A Case Report of Syndrome of Inappropriate Antidiuretic Hormone Induced by Pregabalin

Jung YJ, Lee DY, Kim HW, Park HS, Kim B

The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the most common cause of euvolemic hyponatremia, and many medications have been associated with SIADH. Pregabalin is a drug used for...
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Severe Hypernatremia Caused by Acute Exogenous Salt Intake Combined with Primary Hypothyroidism

Jung WJ, Park SM, Park JM, Rhee H, Kim IY, Lee DW, Lee SB, Seong EY, Kwak IS, Song SH

This report describes a case of severe hypernatremia with a serum sodium concentration of 188.1mmol/L caused by exogenous salt intake. A 26-year-old man diagnosed with Crohn's disease 5 years previously...
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Genetic Variations of Tyrosine Hydroxylase in the Pathogenesis of Hypertension

Lee YH, Kim YG, Moon JY, Kim JS, Jeong KH, Lee TW, Ihm CG, Lee SH

One of the major pathophysiological features of primary hypertension is an inappropriate activation of the sympathetic nervous system, which is mediated by excessive synthesis and secretion of catecholamine into the...
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