Pachyonychia Congenita Type II: A Case Report
Artigo
| IMSEAR
| ID: sea-185965
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.
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Índice:
IMSEAR (Sudeste Asiático)
Ano de publicação:
2014
Tipo de documento:
Artigo
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