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10.1155/2019/4204907 http://scihub22266oqcxt.onion/10.1155/2019/4204907 30867665/?report=reader!6379858!30867665     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Case+Rep+Med 2019 ; 2019 (ä): 4204907 Nephropedia Template TP {{tp|p=30867665|t=2019. Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review |pdf=|usr=}}{{30867665}} gab.com Text Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review JO: Case Rep Med http://www.kidney.de/pget.php?&tw=1&pmid=30867665 #FOAvip Gitelman syndrome is one of the few inherited causes of metabolic alkalosis due to salt losing tubulopathy. It is caused by tubular defects at the level of distal convoluted tubules, mimicking a thiazide-like tumor. It usually presents in late childhood or in teenage as nonspecific weakness, fatigability, polyuria, and polydipsia but very rarely with seizures. It is classically associated with hypokalemia, hypomagnesemia, hypocalciuria, hyperreninemia, and hyperaldosteronism. However, less frequently, it can present with normal magnesium levels. It is even rarer to find normomagnesemic patients of GS who develop seizures as the main complication since hypomagnesemia is considered the principal etiology of abnormal foci of seizure-related brain activity in GS cases. Interestingly, patients with GS are oftentimes diagnosed during pregnancy when the classic electrolyte pattern consistent with GS is noticed. Our case presents GS with normal serum magnesium in a patient, with seizures being the main clinical presentation. We also did a comprehensive literature review of 122 reported cases to show the prevalence of normal magnesium in GS cases and an overview of clinical and biochemical variability in GS. We suggest that further studies and in-depth analysis are required to understand the pathophysiology of seizures in GS patients with both normal and low magnesium levels. Twit Text FOAVip Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review ????Case Rep Med http://www.kidney.de/pget.php?&tw=1&pmid=30867665 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=30867665 #FOAvip English Wikipedia <ref>{{Cite pmid|30867665}}</ref> Gitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic Review #MMPMID30867665 Shahzad MA; Mukhtar M; Ahmed A; Ullah W; Saeed R; Hamid M Case Rep Med 2019[]; 2019 (ä): 4204907 PMID30867665show ga Gitelman syndrome is one of the few inherited causes of metabolic alkalosis due to salt losing tubulopathy. It is caused by tubular defects at the level of distal convoluted tubules, mimicking a thiazide-like tumor. It usually presents in late childhood or in teenage as nonspecific weakness, fatigability, polyuria, and polydipsia but very rarely with seizures. It is classically associated with hypokalemia, hypomagnesemia, hypocalciuria, hyperreninemia, and hyperaldosteronism. However, less frequently, it can present with normal magnesium levels. It is even rarer to find normomagnesemic patients of GS who develop seizures as the main complication since hypomagnesemia is considered the principal etiology of abnormal foci of seizure-related brain activity in GS cases. Interestingly, patients with GS are oftentimes diagnosed during pregnancy when the classic electrolyte pattern consistent with GS is noticed. Our case presents GS with normal serum magnesium in a patient, with seizures being the main clinical presentation. We also did a comprehensive literature review of 122 reported cases to show the prevalence of normal magnesium in GS cases and an overview of clinical and biochemical variability in GS. We suggest that further studies and in-depth analysis are required to understand the pathophysiology of seizures in GS patients with both normal and low magnesium levels. äGitelman Syndrome: A Rare Cause of Seizure Disorder and a Systematic R(epmc).pdf DeepDyve Pubget Overpricing