Results 131 to 140 of about 2,349 (166)
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Advances in Chronic Kidney Disease, 2006
In the past decade our understanding of the etiology and pathophysiology of Gitelman syndrome, an autosomal recessive salt-losing tubular disorder with secondary hypokalemia, has increased considerably through the achievements of molecular genetics and cell physiology.
Nine V A M Knoers
exaly +4 more sources
In the past decade our understanding of the etiology and pathophysiology of Gitelman syndrome, an autosomal recessive salt-losing tubular disorder with secondary hypokalemia, has increased considerably through the achievements of molecular genetics and cell physiology.
Nine V A M Knoers
exaly +4 more sources
Bartter Syndrome and Gitelman Syndrome
Pediatric Clinics of North America, 2019Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. Clinical presentations range from severe antenatal disease to asymptomatic with incidental diagnosis. Hypokalemic hypochloremic metabolic alkalosis is the common feature. Bartter variants may be associated with polyuria and weakness.
Patricia Seo-Mayer
exaly +3 more sources
Gitelman Syndrome and Pregnancy. [PDF]
CKJ: Clinical Kidney Journal, 2012 Gitelman syndrome (GS) is an autosomal-recessive condition characterized by hypokalemia, hypomagnesemia and hypocalciuria. Very little information is available in the literature to guide the management of pregnant patients with GS. We report a case of a 27-year-old woman with GS who became pregnant and despite persistent hypokalemia and hypomagnesemia ...
Moustakakis, Michael N. +1 more
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Bartter's and Gitelman's syndrome
Current Opinion in Pediatrics, 2017Purpose of review The clinical presentations of Bartter's syndrome and Gitelman's syndrome will be reviewed including two most recently described hypokalemic salt-losing tubulopathies. By taking the quite heterogeneous presentations and the apparently different pathophysiologies as the basis, the applicability of the ...
Hannsjörg W, Seyberth +2 more
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Bartter and Gitelman Syndromes
Advances in Pediatrics, 2000Since the initial description in the 1960s of patients with seemingly inherited disorders characterized by hypokalemia and metabolic alkalosis, the pathophysiologic processes underlying Bartter and Gitelman syndromes have generated tremendous study and speculation.
S J, Schurman, L R, Shoemaker
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Acquired Gitelman’s syndrome: an oxymoron?
International Urology and Nephrology, 2010We present the case of a 27-year-old woman with end stage renal disease from Diabetes Mellitus type 1 who had been on hemodialysis for a year. Her father, who was otherwise healthy, was evaluated as a possible living donor. Incidentally, during the workup process, he was identified as having Gitelman's syndrome (GS).
Renu, Bansal, Vinay K, Ranga
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Understanding Bartter Syndrome and Gitelman Syndrome
World Journal of Pediatrics, 2012We aim to review the clinical features of two renal tubular disorders characterized by sodium and potassium wasting: Bartter syndrome and Gitelman syndrome.Selected key references concerning these syndromes were analyzed, together with a PubMed search of the literature from 2000 to 2011.The clinical features common to both conditions and those which ...
Oliver T, Fremont, James C M, Chan
exaly +3 more sources
Magnesium supplementation in Gitelman syndrome
Pediatric Nephrology, 1999The metabolism of potassium and magnesium are closely linked (in situations where potassium and magnesium depletion coexist, magnesium restoration alone is sufficient to correct hypokalemia). Moreover, magnesium deficiency blunts the interplay between circulating calcium and the calciotropic hormones.
A. Bettinelli +5 more
openaire +3 more sources