Keratoderma Hereditariamutilans: A Rare Disorder of Keratinization
Journal Title: International Journal of Health Sciences and Research - Year 2017, Vol 7, Issue 1
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.
Authors and Affiliations
Shikha .
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