Case Report
Year: 2017 | Month: January | Volume: 7 | Issue: 1 | Pages: 326-329
Keratoderma Hereditariamutilans: A Rare Disorder of Keratinization
Shikha1, Mudita Gupta2, Pragya Gupta1
1Postgraduate Student, 2Assistant Professor,
Department of Dermatology, Venereology and Leprosy, Indira Gandh Medical College, Shimla
Corresponding Author: Mudita Gupta
ABSTRACT
Keratoderma hereditariamutilans is a rare, autosomal dominant disorder of keratinization characterized by palmoplantar keratoderma and ainhum-like constrictions. We report herein a 16-year-old deaf –mute girl, since birth with palmoplantar hyperkeratosis with a honeycomb-like appearance, constricting band in her bilateral little finger, starfish keratosis on extensor surface of joints and nail changes.
Key words: Palmoplantar keratoderma, ainhum like.