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10.5005/jp-journals-10005-1377 http://scihub22266oqcxt.onion/10.5005/jp-journals-10005-1377 C5086019!5086019!27843263     free     free     free       Int+J+Clin+Pediatr+Dent 2016 ; 9 (3): 278-80 Nephropedia Template TP {{tp|p=27843263|t=2016. Goldenhar Syndrome: A Case Report with Review |pdf=|usr=}}{{27843263}} gab.com Text Goldenhar Syndrome: A Case Report with Review JO: Int J Clin Pediatr Dent http://www.kidney.de/pget.php?&tw=1&pmid=27843263 #FOAvip Goldenhar syndrome is a rare condition which is characterized by a multitude of anomalies involving craniofacial structures, vertebrae, internal organs and usually occurs unilaterally. The etiology of this syndrome is unclear since it varies genetically and is linked to a plethora of reasons. Herein, we report a case of Goldenhar syndrome with hemifacial microsomia and microtia along with systemic involvement which was clinically and radio-graphically assessed. Many classical signs of the syndrome were present in the patient along with few rare ones. The various aspects of this rare disease have been discussed with emphasis on timely diagnosis and multidisciplinary approach to manage it.How to cite this article: Goswami M, Bhushan U, Jangra B. Goldenhar Syndrome: A Case Report with Review. Int J Clin Pediatr Dent 2016;9(3):278-280. Twit Text FOAVip Goldenhar Syndrome: A Case Report with Review ????Int J Clin Pediatr Dent http://www.kidney.de/pget.php?&tw=1&pmid=27843263 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27843263 #FOAvip English Wikipedia <ref>{{Cite pmid|27843263}}</ref> Goldenhar Syndrome: A Case Report with Review #MMPMID27843263 Goswami M; Bhushan U; Jangra B Int J Clin Pediatr Dent 2016[Jul]; 9 (3): 278-80 PMID27843263show ga Goldenhar syndrome is a rare condition which is characterized by a multitude of anomalies involving craniofacial structures, vertebrae, internal organs and usually occurs unilaterally. The etiology of this syndrome is unclear since it varies genetically and is linked to a plethora of reasons. Herein, we report a case of Goldenhar syndrome with hemifacial microsomia and microtia along with systemic involvement which was clinically and radio-graphically assessed. Many classical signs of the syndrome were present in the patient along with few rare ones. The various aspects of this rare disease have been discussed with emphasis on timely diagnosis and multidisciplinary approach to manage it.How to cite this article: Goswami M, Bhushan U, Jangra B. Goldenhar Syndrome: A Case Report with Review. Int J Clin Pediatr Dent 2016;9(3):278-280. äGoldenhar Syndrome: A Case Report with Review (epmc).pdf DeepDyve Pubget Overpricing