Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report

  • Acharya S
  • Panda S
  • Singh Dhull K
  • et al.
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Abstract

Gorlin's syndrome is a rare disorder transmitted as an autosomal dominant trait. It is characterized by multiple disorders involving multiple systems. We present a case of 11-year-old male child presenting with multiple odontogenic keratocyst to the dental clinic. Retrograde diagnosis of Gorlin-Goltz syndrome was made after clinical and radiological investigation. How to cite this article: Acharya S, Panda S, Dhull KS, Sahoo SR, Ray P. Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report. Int J Clin Pediatr Dent 2013;6(3):208-212.

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APA

Acharya, S., Panda, S., Singh Dhull, K., & Sahoo, R. S. (2013). Gorlin Syndrome with Bilateral Polydactyly: A Rare Case Report. International Journal of Clinical Pediatric Dentistry, 6(3), 208–212. https://doi.org/10.5005/jp-journals-10005-1221

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