Indian Journal of Paediatric Dermatology

CASE REPORT
Year
: 2015  |  Volume : 16  |  Issue : 2  |  Page : 108--109

Keratoderma hereditarium mutilans (Vohwinkel«SQ»s syndrome)


Sweta Hasmukh Rambhia, Niranjana Raj, Madhu Suguna Madan, Bhanu Prakash 
 Department of Dermatology, Vydehi Institute of Medical College and Research Centre, Bengaluru, Karnataka, India

Correspondence Address:
Sweta Hasmukh Rambhia
Umarshi Building, 109, SV Road, Malad West, Mumbai 400 064, Maharashtra
India

Vohwinkel«SQ»s syndrome is an autosomal dominant type of palmoplantar keratoderma characterized by honeycomb appearance, pseudoainhum leading to autoamputation, stellate keratosis on knuckles, and associated with sensorineural deafness.An Ichthyotic variant is recently described .We report a rare case of Vohwinkels syndrome with ichthyosis.


How to cite this article:
Rambhia SH, Raj N, Madan MS, Prakash B. Keratoderma hereditarium mutilans (Vohwinkel's syndrome).Indian J Paediatr Dermatol 2015;16:108-109


How to cite this URL:
Rambhia SH, Raj N, Madan MS, Prakash B. Keratoderma hereditarium mutilans (Vohwinkel's syndrome). Indian J Paediatr Dermatol [serial online] 2015 [cited 2020 Aug 8 ];16:108-109
Available from: http://www.ijpd.in/article.asp?issn=2319-7250;year=2015;volume=16;issue=2;spage=108;epage=109;aulast=Rambhia;type=0