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10.1093/omcr/omv065 http://scihub22266oqcxt.onion/10.1093/omcr/omv065 C4672230!4672230 !26664725     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26664725 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Oxf+Med+Case+Reports 2015 ; 2015 (12 ): 367-70 Nephropedia Template TP {{tp|p=26664725 |t=2015. Report of two Syrian siblings with Mulibrey nanism |pdf=|usr=}}{{26664725 }} gab.com Text Report of two Syrian siblings with Mulibrey nanism JO: Oxf Med Case Reports http://www.kidney.de/pget.php?&tw=1&pmid=26664725 #FOAvip Mulibrey (MUscle-LIver-BRain-EYe) nanism is a rare autosomal recessive disease characterized by growth failure, dysmorphic features and a wide range of abnormalities affecting multiple organ systems. This report is the first to present two cases of Mulibrey nanism affecting two siblings from Syria. Mulibrey nanism can be suspected clinically due to the distinctive features of the patients. The aim of this report is to document the presence of Mulibrey nanism in Syria and to familiarize physicians in and out of Syria with this rare disease and encourage them to develop high clinical suspicion if faced with patients with similar presentations. Twit Text FOAVip Report of two Syrian siblings with Mulibrey nanism ????Oxf Med Case Reports http://www.kidney.de/pget.php?&tw=1&pmid=26664725 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26664725 #FOAvip English Wikipedia <ref>{{Cite pmid|26664725 }}</ref> Report of two Syrian siblings with Mulibrey nanism #MMPMID26664725 Al Saadi T ; Alkhatib M ; Turk T ; Turkmani K ; Abbas F ; Khouri L Oxf Med Case Reports 2015[Dec]; 2015 (12 ): 367-70 PMID26664725 show ga Mulibrey (MUscle-LIver-BRain-EYe) nanism is a rare autosomal recessive disease characterized by growth failure, dysmorphic features and a wide range of abnormalities affecting multiple organ systems. This report is the first to present two cases of Mulibrey nanism affecting two siblings from Syria. Mulibrey nanism can be suspected clinically due to the distinctive features of the patients. The aim of this report is to document the presence of Mulibrey nanism in Syria and to familiarize physicians in and out of Syria with this rare disease and encourage them to develop high clinical suspicion if faced with patients with similar presentations. äReport of two Syrian siblings with Mulibrey nanism (epmc).pdf DeepDyve Pubget Overpricing