Waardenburg syndrome type 2 Gaikwad RP, Mukherjee S, Saha A, Naphade P, - J Indian Prosthodont Soc

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Waardenburg syndrome type 2 Rohini P Gaikwad¹, Samipa Mukherjee², Abhijit Saha³, Poonam Naphade⁴ ¹ Department of Dermatology, M.I.M.E.R Medical College, Talegaon Dabhade, Maharashtra, India ² Department of Dermatology, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India ³ Pediatric Dermatology Unit, Rita Skin Foundation, Salt Lake, Kolkata, West Bengal, India ⁴ Consultant Dermatologist, Pushp Clinic, Pune, Maharashtra, India Correspondence Address: Samipa Mukherjee, Department of Dermatology, Bangalore Medical College and Research Institute, Bengaluru 560 002, Karnataka India Source of Support: None, Conflict of Interest: None DOI: 10.4103/2319-7250.158302

Waardenburg syndrome is a rare disorder characterized by sensorineural deafness with pigmentary anomalies and defects of the neural crest cells transmitted in an autosomal dominant fashion. Depending on the deformities caused by the disease some patients may need a multi-disciplinary approach while some may not need any treatment. Based on associated characteristics found and variable mutations there are four types of the syndrome. Here, we report a case of an 11-year-old male child who was found to have this disorder when a school survey was conducted at the school for deaf and dumb. It was also noted that there was generalized follicular hyperkeratosis, which could be a co-incidental finding.

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