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Case Report

KY Guruprasad1 , Mohammed Waseem Javed2 

1. Professor & Head, 2 Postgraduate Student, Dept of Dermatology, Venereology & Leprosy, K.B.N. Institute of Medical Sciences, Kalaburagi.

Address for correspondence

Dr K Y Guruprasad

Professor and Head Department of Dermatology, KBN Institute of Medical Sciences, Kalaburagi gprasadyel@rediffmail.com

Received Date: 2017-03-12,
Accepted Date: 2017-04-20,
Published Date: 2017-04-30
Year: 2017, Volume: 7, Issue: 2, Page no. 83-86, DOI: 10.26463/rjms.7_2_2
Views: 980, Downloads: 9
Licensing Information:
CC BY NC 4.0 ICON
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0.
Abstract

Olmsted syndrome is a rare keratinisation disorder, characterised by mutilating palmoplantar keratoderma with peri-orificial hyperkeratosis. Till now around 73 cases have been reported. We are reporting a case of 3 year old female child, with keratoderma of palms and soles since birth along with peri-orificial hyperkeratosis, flexion deformity of digits of palms, hypotrichosis and onychodystrophy. There was no history of hyperhidrosis, no dental abnormalities and no sensorineural hearing loss. Hence the diagnosis of Olmsted syndrome was made.

<p>Olmsted syndrome is a rare keratinisation disorder, characterised by mutilating palmoplantar keratoderma with peri-orificial hyperkeratosis. Till now around 73 cases have been reported. We are reporting a case of 3 year old female child, with keratoderma of palms and soles since birth along with peri-orificial hyperkeratosis, flexion deformity of digits of palms, hypotrichosis and onychodystrophy. There was no history of hyperhidrosis, no dental abnormalities and no sensorineural hearing loss. Hence the diagnosis of Olmsted syndrome was made.</p>
Keywords
Olmsted syndrome, Palmoplantar Keratoderma, Onychodystrophy
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