Pachyonychia Congenita Type II: A Case Report Reddy V. Sindhuri, PG Student, Latha M. Madhavi*, Associate Professor, Saheb D. Masthan, Professor Department of Dermatology, Santhiram Medical College and Hospital, Nandyal, Andhra Pradesh, India *Corresponding author email id: vc.madhavi@gmail.com
Online published on 11 November, 2014. Abstract Pachyonychia congenita type II is an autosomal dominant inherited rare genodermatosis characterized by dystrophic wedge shaped thickened nails with subungual hyperkeratosis, symmetric palmoplantar keratoderma, steatocystoma multiplex. Here we report a 23-year-old male with characteristic features of dystrophic nails, palmoplantar keratoderma, steatocystoma multiplex, follicular hyperkeratotic papules and history of natal teeth at birth. Top Keywords Dystrophic nails, Palmoplantar keratoderma, Natal teeth, Steatocystoma multiplex. Top |