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A Rare Syndrome Resembling Scleroderma: Huriez Syndrome
Huriez syndrome, also referred to as “sclerotylosis,” is a rare autosomal dominant genodermatosis characterized by the triad of congenital scleroatrophy of the distal extremities, palmoplantar keratoderma, and hypoplastic nails. The development of aggressive squamous cell carcinoma (SCC) arising in...
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| I publikationen: | Skin Appendage Disord |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
S. Karger AG
2018
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5939708/ https://ncbi.nlm.nih.gov/pubmed/29765964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000479036 |
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