Goldenhar Syndrome–A Case Report

Journal Title: Cumhuriyet Dental Journal - Year 2019, Vol 22, Issue 1

Abstract

Goldenhar Syndrome also called as facio-auriculo-vertebral dysplasia, is a rare syndrome developing from first and second pharyngeal arches during Blastogenesis. It was described by Maurice Goldenhar in 1952. It is characterised by presence of epibulbar dermoids, ear malformations, vertebral anomalies, unilateral facial hypoplasia, and sometimes internal systemic complications. As the molecular basis for Goldenhar Syndrome is unclear, early detection and screening for complications would help the patients to have a normal life.

Authors and Affiliations

Vidya Holla, Raghavendra Kini, Prassana Kumar Rao, Roopashri Kashyap, Devika Shetty, Kamakshi Jha

Keywords

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  • EP ID EP481400
  • DOI 10.7126/cumudj.454491
  • Views 106
  • Downloads 0

How To Cite

Vidya Holla, Raghavendra Kini, Prassana Kumar Rao, Roopashri Kashyap, Devika Shetty, Kamakshi Jha (2019). Goldenhar Syndrome–A Case Report. Cumhuriyet Dental Journal, 22(1), 131-135. https://europub.co.uk./articles/-A-481400