Non epidermolytic PPK– a case report

dc.contributor.author	Kikkeri, Naveen Narayanashetty
dc.contributor.author	Pai, Varadraj V.
dc.contributor.author	Sori, Tukaram
dc.date.accessioned	2013-02-08T11:44:51Z
dc.date.available	2013-02-08T11:44:51Z
dc.date.issued	2012-02-19
dc.identifier.citation	Novel Science International Journal of Medical Science. 2012; 1: 17-18.	en_US
dc.identifier.issn	2278-0025
dc.identifier.uri	http://hdl.handle.net/123456789/352
dc.description.abstract	Non epidermolytic PPK is an autosomal dominant keratoderma principally involving the soles with onset in infancy or the first few years of life. It also is known as Brunauer-Fohs-Siemens syndrome, Wachter-type focal NEPPK, and PPK areata/striata .Here we are presenting non epidermolytic PPK without family history of similar lesion, which is very rarely reported.	en_US
dc.language.iso	en	en_US
dc.publisher	Novel Science	en_US
dc.subject	Non epidermolytic PPK
dc.title	Non epidermolytic PPK– a case report	en_US
dc.type	Article	en_US