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10.1155/2015/435967 http://scihub22266oqcxt.onion/10.1155/2015/435967 C4617704!4617704!26635984     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 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 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Case+Rep+Ophthalmol+Med 2015 ; 2015 (ä): ä Nephropedia Template TP {{tp|p=26635984|t=2015. Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract |pdf=|usr=}}{{26635984}} gab.com Text Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract JO: Case Rep Ophthalmol Med http://www.kidney.de/pget.php?&tw=1&pmid=26635984 #FOAvip Craniofacial microsomia (CFM) includes a spectrum of malformations primarily involving structures derived from the first and second branchial arches. Patients with hemifacial microsomia and epibulbar dermoids are said to have Goldenhar syndrome (GHS). Four-month-old boy with whitish pupillary reflex presented with the features of GHS in pediatric ophthalmology clinic. The child had ocular and auricular manifestations. There were no vertebral anomalies, but he had bilateral congenital cataract. The peculiarity of this case is the presence of the bilateral total congenital cataract, in association with CFM. There is absence of epibulbar dermoid or lipodermoid in the eyes, although the child had features of GHS. In addition to it, anesthetic intubation was smooth in this case. Any case diagnosed with CFM and/or GHS needs treatment through multidisciplinary approach, consultation in ophthalmology department is one of them. Twit Text FOAVip Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract ????Case Rep Ophthalmol Med http://www.kidney.de/pget.php?&tw=1&pmid=26635984 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26635984 #FOAvip English Wikipedia <ref>{{Cite pmid|26635984}}</ref> Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract #MMPMID26635984 Shrestha UD; Adhikari S Case Rep Ophthalmol Med 2015[]; 2015 (ä): ä PMID26635984show ga Craniofacial microsomia (CFM) includes a spectrum of malformations primarily involving structures derived from the first and second branchial arches. Patients with hemifacial microsomia and epibulbar dermoids are said to have Goldenhar syndrome (GHS). Four-month-old boy with whitish pupillary reflex presented with the features of GHS in pediatric ophthalmology clinic. The child had ocular and auricular manifestations. There were no vertebral anomalies, but he had bilateral congenital cataract. The peculiarity of this case is the presence of the bilateral total congenital cataract, in association with CFM. There is absence of epibulbar dermoid or lipodermoid in the eyes, although the child had features of GHS. In addition to it, anesthetic intubation was smooth in this case. Any case diagnosed with CFM and/or GHS needs treatment through multidisciplinary approach, consultation in ophthalmology department is one of them. äCraniofacial Microsomia: Goldenhar Syndrome in Association with Bilate(epmc).pdf DeepDyve Pubget Overpricing