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10.1002/jcu.22386 http://scihub22266oqcxt.onion/10.1002/jcu.22386 27492745!ä!27492745 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       J+Clin+Ultrasound 2017 ; 45 (3): 168-170 Nephropedia Template TP {{tp|p=27492745|t=2017. A multidisciplinary approach to prenatal treatment of congenital long QT syndrome |pdf=|usr=}}{{27492745}} gab.com Text A multidisciplinary approach to prenatal treatment of congenital long QT syndrome JO: J Clin Ultrasound http://www.kidney.de/pget.php?&tw=1&pmid=27492745 #FOAvip A 27-week fetus evaluated for bradycardia and hydrops was found to have anti-SSA-negative 2 degrees atrioventricular block and ventricular tachycardia. A presumptive diagnosis of fetal long QT syndrome was made. Transplacental pharmacotherapy with intravenous magnesium and lidocaine restored sinus rhythm. At 30 6/7 weeks, the infant was delivered due to premature labor. Despite postnatal treatment with mexiletine and propranolol, she developed torsades de pointes. Ultimately, a de novo KCNH2 G628S mutation was diagnosed. She received an implantable cardiac defibrillator at 5 months of age. Early diagnosis and a multidisciplinary approach allowed successful in utero treatment and anticipatory postnatal management. (c) 2016 Wiley Periodicals, Inc. J Clin Ultrasound 45:168-170, 2017. Twit Text FOAVip A multidisciplinary approach to prenatal treatment of congenital long QT syndrome ????J Clin Ultrasound http://www.kidney.de/pget.php?&tw=1&pmid=27492745 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27492745 #FOAvip English Wikipedia <ref>{{Cite pmid|27492745}}</ref> A multidisciplinary approach to prenatal treatment of congenital long QT syndrome #MMPMID27492745 Crimmins S; Vashit S; Doyle L; Harman C; Turan O; Turan S J Clin Ultrasound 2017[Mar]; 45 (3): 168-170 PMID27492745show ga A 27-week fetus evaluated for bradycardia and hydrops was found to have anti-SSA-negative 2 degrees atrioventricular block and ventricular tachycardia. A presumptive diagnosis of fetal long QT syndrome was made. Transplacental pharmacotherapy with intravenous magnesium and lidocaine restored sinus rhythm. At 30 6/7 weeks, the infant was delivered due to premature labor. Despite postnatal treatment with mexiletine and propranolol, she developed torsades de pointes. Ultimately, a de novo KCNH2 G628S mutation was diagnosed. She received an implantable cardiac defibrillator at 5 months of age. Early diagnosis and a multidisciplinary approach allowed successful in utero treatment and anticipatory postnatal management. (c) 2016 Wiley Periodicals, Inc. J Clin Ultrasound 45:168-170, 2017. |Adult[MESH] |Electrocardiography[MESH] |Female[MESH] |Heart Rate Determination/methods[MESH] |Humans[MESH] |Lidocaine/therapeutic use[MESH] |Long QT Syndrome/*diagnosis/embryology/*therapy[MESH] |Magnesium/therapeutic use[MESH] |Monitoring, Physiologic/methods[MESH] |Pregnancy[MESH] |Prenatal Diagnosis/*methods[MESH] |Ultrasonography, Prenatal[MESH]A multidisciplinary approach to prenatal treatment of congenital long (epmc).pdf DeepDyve Pubget Overpricing