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10.3233/PGE-13069 http://scihub22266oqcxt.onion/10.3233/PGE-13069 C5020980!5020980!27625859     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       J+Pediatr+Genet 2013 ; 2 (4): 197-201 Nephropedia Template TP {{tp|p=27625859|t=2013. Constitutional trisomy 8 mosaicism syndrome: case report and review |pdf=|usr=}}{{27625859}} gab.com Text Constitutional trisomy 8 mosaicism syndrome: case report and review JO: J Pediatr Genet http://www.kidney.de/pget.php?&tw=1&pmid=27625859 #FOAvip Trisomy 8 mosaicism (Warkany syndrome) is a rare viable condition with variable phenotypes, ranging from mild dysmorphic features to severe malformations. Karyotyping and fluorescence in-situ hybridization potentially help detecting this low mosaic clone to confirm the diagnosis of patients with classical and unusual clinical presentations. This report reviews few previous cases to describe our case - a boy who had trisomy 8 mosaicism with severe dysmorphic features, born to a consanguineous Arabic couple. This study concludes that careful cytogenetic diagnoses of trisomy 8 mosaicism is essential for appropriate management and follow up of this rare disorder. Twit Text FOAVip Constitutional trisomy 8 mosaicism syndrome: case report and review ????J Pediatr Genet http://www.kidney.de/pget.php?&tw=1&pmid=27625859 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27625859 #FOAvip English Wikipedia <ref>{{Cite pmid|27625859}}</ref> Constitutional trisomy 8 mosaicism syndrome: case report and review #MMPMID27625859 Udayakumar AM; Al-Kindy A J Pediatr Genet 2013[Dec]; 2 (4): 197-201 PMID27625859show ga Trisomy 8 mosaicism (Warkany syndrome) is a rare viable condition with variable phenotypes, ranging from mild dysmorphic features to severe malformations. Karyotyping and fluorescence in-situ hybridization potentially help detecting this low mosaic clone to confirm the diagnosis of patients with classical and unusual clinical presentations. This report reviews few previous cases to describe our case - a boy who had trisomy 8 mosaicism with severe dysmorphic features, born to a consanguineous Arabic couple. This study concludes that careful cytogenetic diagnoses of trisomy 8 mosaicism is essential for appropriate management and follow up of this rare disorder. äConstitutional trisomy 8 mosaicism syndrome: case report and review (epmc).pdf DeepDyve Pubget Overpricing