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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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| Main Authors: | , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2013
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| Fag: | |
| Online adgang: | 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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