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10.3233/PGE-2012-010 http://scihub22266oqcxt.onion/10.3233/PGE-2012-010 C5020920!5020920!27625802     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Pediatr+Genet 2012 ; 1 (1): 55-8 Nephropedia Template TP {{tp|p=27625802|t=2012. Esophageal atresia and anal atresia in a newborn with heterotaxia combined with other congenital defects |pdf=|usr=}}{{27625802}} gab.com Text Esophageal atresia and anal atresia in a newborn with heterotaxia combined with other congenital defects JO: J Pediatr Genet http://www.kidney.de/pget.php?&tw=1&pmid=27625802 #FOAvip Heterotaxia (HTX) is a heterogeneous group of laterality defects characterized by abnormal discordance of asymmetric thoracic and abdominal organs. Esophageal anomalies occur rarely in HTX cases although additional defects associated with esophageal atresia are common. We report on a rare case of a neonate with HTX and multiple congenital malformations as well as specific facial dysmorphism, corresponding only to a few cases described in literature. Clinical examination of the proband revealed esophageal atresia with distal tracheoesophageal fistula, anal atresia, abdominal situs inversus, dextrocardia with complex congenital heart defect and left lung agenesis. A complex genetic analysis revealed no genetic abnormalities. Despite extensive diagnostic procedures, the cause of the laterality sequence disruption remains unclear, indicating its multifactorial etiology. Twit Text FOAVip Esophageal atresia and anal atresia in a newborn with heterotaxia combined with other congenital defects ????J Pediatr Genet http://www.kidney.de/pget.php?&tw=1&pmid=27625802 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27625802 #FOAvip English Wikipedia <ref>{{Cite pmid|27625802}}</ref> Esophageal atresia and anal atresia in a newborn with heterotaxia combined with other congenital defects #MMPMID27625802 Smigiel R; Misiak B; Golebiowski W; Lebioda A; Dorobisz U; Zielinska M; Patkowski D J Pediatr Genet 2012[Mar]; 1 (1): 55-8 PMID27625802show ga Heterotaxia (HTX) is a heterogeneous group of laterality defects characterized by abnormal discordance of asymmetric thoracic and abdominal organs. Esophageal anomalies occur rarely in HTX cases although additional defects associated with esophageal atresia are common. We report on a rare case of a neonate with HTX and multiple congenital malformations as well as specific facial dysmorphism, corresponding only to a few cases described in literature. Clinical examination of the proband revealed esophageal atresia with distal tracheoesophageal fistula, anal atresia, abdominal situs inversus, dextrocardia with complex congenital heart defect and left lung agenesis. A complex genetic analysis revealed no genetic abnormalities. Despite extensive diagnostic procedures, the cause of the laterality sequence disruption remains unclear, indicating its multifactorial etiology. äEsophageal atresia and anal atresia in a newborn with heterotaxia comb(epmc).pdf DeepDyve Pubget Overpricing