Goldenhar syndrome was discovered by Maurice Goldenhar way back in 1850 since then it is famous after his name as Goldenhar Syndrome. It is a Congenital presence of a limbal dermoid with congenital syndrome complex entity which was described as preauricular skin tag or preauricular appendage.
Sometimes the presence of a squint or 3 infants born in the middle east in ophthalmology or cog coloboma of a lid may also be seen, though it is very rare. G.H.S is also termed as oculo-auriculo-vertebral (OAV) syndrome with associated craniofacial dysplasia involving head and face particularly ear nose soft plate and mandible however, these additional benefits in G.H.S occur in only 5 to 15 percent of cases to incomplete development of 1 st and 2 nd bronchial arch due to defect in genes and are autosomal dominant or recessive however almost all cases of G.H.S have normal vision and intelligence.…
