Epidermolysis bullosa pruriginosa: a report of two cases

dc.contributor.author	Pai, Varadraj V.
dc.contributor.author	Sori, Tukaram
dc.contributor.author	Kikkeri, Naveen Narayanashetty
dc.contributor.author	Athanikar, Sharatchandra B.
dc.contributor.author	Rai, Vijetha
dc.contributor.author	Dinesh, U. S.
dc.date.accessioned	2014-05-12T18:32:48Z
dc.date.available	2014-05-12T18:32:48Z
dc.date.issued	2014-01
dc.identifier.citation	Indian Dermatology Online Journal. 2014 Jan-Mar; 5(1): 44-47.	en_US
dc.identifier.issn	2229-5178, 2249-5673
dc.identifier.uri	http://hdl.handle.net/123456789/534
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Wolters Kluwer - Medknow	en_US
dc.subject	Epidermolysis bullosa pruriginosa	en_US
dc.title	Epidermolysis bullosa pruriginosa: a report of two cases	en_US
dc.type	Article	en_US