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10.1136/bcr.02.2012.5888 http://scihub22266oqcxt.onion/10.1136/bcr.02.2012.5888 C3448348!3448348!22744244     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMJ+Case+Rep 2012 ; 2012 (ä): ä Nephropedia Template TP {{tp|p=22744244|t=2012. Classic Bartter syndrome: a rare cause of failure to thrive in a child |pdf=|usr=}}{{22744244}} gab.com Text Classic Bartter syndrome: a rare cause of failure to thrive in a child JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=22744244 #FOAvip Bartter syndrome is a group of rare autosomal-recessive disorders caused by a defect in distal tubule transport of sodium and chloride. Blood gases and plasma electrolytes raise suspicion of this diagnosis and the definitive diagnosis is made by genetic study. Early treatment improves prognosis. The authors present the case of an 11-month-old child with early failure to thrive and severe regurgitation. Blood gases revealed hypochloraemic metabolic alkalosis, hyponatraemia and hypokalaemia. Blood pressure was normal and polyuria was documented. She began therapy with potassium chloride supplementation and indomethacin. There was clinical improvement and plasma potassium and bicarbonate normalised. The molecular study confirmed it was the classic form of Bartter syndrome. Despite being rare in clinical practice, which may lead to unnecessary medical investigation and diagnosis delay, in a child with failure to thrive, hypochloraemic metabolic alkalosis and hypokalaemia, this diagnosis must be considered. Twit Text FOAVip Classic Bartter syndrome: a rare cause of failure to thrive in a child ????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=22744244 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=22744244 #FOAvip English Wikipedia <ref>{{Cite pmid|22744244}}</ref> Classic Bartter syndrome: a rare cause of failure to thrive in a child #MMPMID22744244 Vieira H; Mendes L; Mendes P; da Silva JE BMJ Case Rep 2012[]; 2012 (ä): ä PMID22744244show ga Bartter syndrome is a group of rare autosomal-recessive disorders caused by a defect in distal tubule transport of sodium and chloride. Blood gases and plasma electrolytes raise suspicion of this diagnosis and the definitive diagnosis is made by genetic study. Early treatment improves prognosis. The authors present the case of an 11-month-old child with early failure to thrive and severe regurgitation. Blood gases revealed hypochloraemic metabolic alkalosis, hyponatraemia and hypokalaemia. Blood pressure was normal and polyuria was documented. She began therapy with potassium chloride supplementation and indomethacin. There was clinical improvement and plasma potassium and bicarbonate normalised. The molecular study confirmed it was the classic form of Bartter syndrome. Despite being rare in clinical practice, which may lead to unnecessary medical investigation and diagnosis delay, in a child with failure to thrive, hypochloraemic metabolic alkalosis and hypokalaemia, this diagnosis must be considered. äClassic Bartter syndrome: a rare cause of failure to thrive in a child(epmc).pdf DeepDyve Pubget Overpricing