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Pachyonychia congenita tarda: A rare case report

Pachyonychia congenita is a rare, but well-characterized autosomal dominant disorder of keratinization. It usually begins within the first few months of life. Here, we are presenting a rare case, which started at the age of 10 years of life and is known as pachyonychia congenita tarda. The case is b...

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Detalhes bibliográficos
Main Authors: Moger, Ganapathi, Shashikanth, M. C., Chandrashekar, K. T., Kurein, Sophia
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3793574/
https://ncbi.nlm.nih.gov/pubmed/24124319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.118374
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