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Case Report Volume 8 Issue 1
Goldenhar Syndrome
Anubhav Chauhan, Shveta Chauhan
Received: January 01, 1971 | Published: February 8, 2018
Citation: Chauhan A, Chauhan S (2018) Goldenhar Syndrome. Adv Ophthalmol Vis Syst 8(2): 00265. DOI: 10.15406/aovs.2018.08.00265
Abstract
Goldenhar syndrome is a hereditary condition which is characterized by preauricular appendages, epibulbar dermoids, along with anomalies of the heart, kidney, and vertebral, central nervous and gastrointestinal system. We report a case of Goldenhar syndrome in a 7-years-old male patient who presented with limbal dermoid, pre auricular tag, microtia and mandibular hypoplasia. We AIM to report this case, given the rarity of this syndrome, and classical signs seen in our patient.
Keywords: Goldenhar, Ocular, Ear, Hereditary, Preauricular appendages, Epibulbar dermoids, Microtia, Mandibular hypoplasia, Eye anomalies, Microphthalmia
©2018 Chauhan, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.