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International Journal of Applied Dental Sciences
  • Printed Journal
  • Indexed Journal
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P-ISSN: 2394-7489, E-ISSN: 2394-7497
ICV 2019: 92.11

2022, Vol. 8 Issue 3, Part B

A rare genetic disorder: Waardenburg syndrome

AUTHOR(S): Dr. Pulkita Prakash, Dr Amitabh Kumar Sinha and Dr. Anmol Ratan
ABSTRACT:Waardenburg syndrome is an inherited autosomal dominant disorder consists group of rare genetic conditions. Mutation in the PAX3, MITF, SOX10 and SNAI2 genes are known as main cause for it. There are four types of Waardenburg syndrome differing in phenotypic characteristics are described. This syndrome is characterized by congenital deafness or some degree of hearing loss, different color of eyes with various degree of depigmentation of skin and hair, increased inter-canthal distance, Dystopia Canthorum. In this report a case has been discussed of finding a 30 years old male patient with Waardenburg syndrome.
Pages: 116-117  |  595 Views  194 Downloads


International Journal of Applied Dental Sciences
How to cite this article:
Dr. Pulkita Prakash, Dr Amitabh Kumar Sinha, Dr. Anmol Ratan. A rare genetic disorder: Waardenburg syndrome. Int J Appl Dent Sci 2022;8(3):116-117. DOI: https://doi.org/10.22271/oral.2022.v8.i3b.1594
International Journal of Applied Dental Sciences

International Journal of Applied Dental Sciences

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International Journal of Applied Dental Sciences