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Poikiloderma a varied presentation - Huriez syndrome
Huriez syndrome is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma (PPK) and hypoplastic nails. We report the case of a 25 year old male, with nonfamilial Huriez syndrome.
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| Publicat a: | Indian Dermatol Online J |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4314883/ https://ncbi.nlm.nih.gov/pubmed/25657913 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.148929 |
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