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10.7860/JCDR/2016/21586.8811 http://scihub22266oqcxt.onion/10.7860/JCDR/2016/21586.8811 C5198416!5198416!28050463     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       J+Clin+Diagn+Res 2016 ; 10 (11): SD01-2 Nephropedia Template TP {{tp|p=28050463|t=2016. Cardiofaciocutaneous Syndrome: Case Report of a Rare Disorder |pdf=|usr=}}{{28050463}} gab.com Text Cardiofaciocutaneous Syndrome: Case Report of a Rare Disorder JO: J Clin Diagn Res http://www.kidney.de/pget.php?&tw=1&pmid=28050463 #FOAvip Cardiofaciocutaneous syndrome or CFC syndrome is a rare genetic disorder first described in 1986. It is one of the RASopathies involving multiple organs particularly the heart, skin and face affecting males and females equally. The phenotypic features overlap with 2 other conditions, the Noonan and Costello syndrome. We report on a 22-month-old boy with CFC syndrome presenting with typical craniofacial appearance, heart defects, ectodermal abnormalities, growth failure and developmental delay. Estimated population of affected individuals worldwide is a few hundreds. Twit Text FOAVip Cardiofaciocutaneous Syndrome: Case Report of a Rare Disorder ????J Clin Diagn Res http://www.kidney.de/pget.php?&tw=1&pmid=28050463 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28050463 #FOAvip English Wikipedia <ref>{{Cite pmid|28050463}}</ref> Cardiofaciocutaneous Syndrome: Case Report of a Rare Disorder #MMPMID28050463 Seth S; Biswas T; Biswas B; Roy A; Datta AK J Clin Diagn Res 2016[Nov]; 10 (11): SD01-2 PMID28050463show ga Cardiofaciocutaneous syndrome or CFC syndrome is a rare genetic disorder first described in 1986. It is one of the RASopathies involving multiple organs particularly the heart, skin and face affecting males and females equally. The phenotypic features overlap with 2 other conditions, the Noonan and Costello syndrome. We report on a 22-month-old boy with CFC syndrome presenting with typical craniofacial appearance, heart defects, ectodermal abnormalities, growth failure and developmental delay. Estimated population of affected individuals worldwide is a few hundreds. äCardiofaciocutaneous Syndrome: Case Report of a Rare Disorder (epmc).pdf DeepDyve Pubget Overpricing