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10.4103/1817-1745.174437 http://scihub22266oqcxt.onion/10.4103/1817-1745.174437 C4770649!4770649!26962343     free     free     free Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Pediatr+Neurosci 2015 ; 10 (4): 359-61 Nephropedia Template TP {{tp|p=26962343|t=2015. Delayed diagnosis of Gorlin syndrome: Learning from mistakes!|pdf=|usr=}}{{26962343}} gab.com Text Delayed diagnosis of Gorlin syndrome: Learning from mistakes! JO: J Pediatr Neurosci http://www.kidney.de/pget.php?&tw=1&pmid=26962343 #FOAvip Gorlin syndrome (GS) is a rare inherited multisystem disorder with predisposition to basal cell carcinomas and various other neoplasms. Characteristic features include falx calcification, multiple odontogenic keratocysts (OKCs), early onset medulloblastoma, craniofacial and skeletal malformations, cardiac and ovarian fibroma. We present a case of GS in a 9-year-old girl with recurrent dental infections which was overlooked for 8 years. Diagnosis was finally suggested by the incidental detection of multiple OKCs and ovarian fibromas on follow-up magnetic resonance imaging performed for surveillance of previous operated brain tumor. Twit Text FOAVip Delayed diagnosis of Gorlin syndrome: Learning from mistakes!????J Pediatr Neurosci http://www.kidney.de/pget.php?&tw=1&pmid=26962343 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26962343 #FOAvip English Wikipedia <ref>{{Cite pmid|26962343}}</ref> Delayed diagnosis of Gorlin syndrome: Learning from mistakes! #MMPMID26962343 Ramanathan S; Kumar D; Al Heidous M; Palaniappan Y J Pediatr Neurosci 2015[Oct]; 10 (4): 359-61 PMID26962343show ga Gorlin syndrome (GS) is a rare inherited multisystem disorder with predisposition to basal cell carcinomas and various other neoplasms. Characteristic features include falx calcification, multiple odontogenic keratocysts (OKCs), early onset medulloblastoma, craniofacial and skeletal malformations, cardiac and ovarian fibroma. We present a case of GS in a 9-year-old girl with recurrent dental infections which was overlooked for 8 years. Diagnosis was finally suggested by the incidental detection of multiple OKCs and ovarian fibromas on follow-up magnetic resonance imaging performed for surveillance of previous operated brain tumor. äDelayed diagnosis of Gorlin syndrome: Learning from mistakes!(epmc).pdf DeepDyve Pubget Overpricing