| Literature DB >> 24616855 |
Varadraj Vasant Pai1, Tukaram Sori2, Kikkeri Narayanshetty Naveen3, Sharatchandra Bhimrao Athanikar3, Vijetha Rai3, Dinesh Udupi Shastry4.
Abstract
Epidermolysis bullosa (EB) pruriginosa is a very rare pattern of dystrophic EB caused by type VII collagen gene mutation, with distinctive clinico-pathological features. It is characterized by nodular prurigo-like lichenified lesions, nail dystrophy, and variable presence of albopapuloid lesions. We report two such cases.Entities:
Keywords: Bullosa; epidermolysis; pruriginosa
Year: 2014 PMID: 24616855 PMCID: PMC3937487 DOI: 10.4103/2229-5178.126030
Source DB: PubMed Journal: Indian Dermatol Online J ISSN: 2229-5178