Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login 
Home Print this page Email this page Small font size Default font size Increase font size Users Online: 217
CASE REPORT
Year : 2015  |  Volume : 16  |  Issue : 2  |  Page : 108-109

Keratoderma hereditarium mutilans (Vohwinkel's syndrome)


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
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2319-7250.152137

Rights and Permissions

Vohwinkel'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.


[FULL TEXT] [PDF]*
Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed1711    
    Printed22    
    Emailed0    
    PDF Downloaded198    
    Comments [Add]    

Recommend this journal