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Epidermolysis bullosa pruriginosa: A report of two cases

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...

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Main Authors: Varadraj Vasant Pai (Author), Tukaram Sori (Author), Kikkeri Narayanshetty Naveen (Author), Sharatchandra Bhimrao Athanikar (Author), Vijetha Rai (Author), Dinesh Udupi Shastry (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2014-01-01T00:00:00Z.
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Summary: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.
Item Description:2229-5178
10.4103/2229-5178.126030

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