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A Familial Poikiloderma-Like Cutaneous Amyloidosis
Familial poikiloderma-like cutaneous amyloidosis(FPLCA) is a rare, generalized but genetic dyschromic skin disorder characterized by amyloid deposits in dermis due to defective DNA repair secondary to sunlight damage. Clinically, it presents with diffuse brownish pigmentation with hypo-pigmented mac...
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| I publikationen: | Indian J Dermatol |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Medknow Publications & Media Pvt Ltd
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4248533/ https://ncbi.nlm.nih.gov/pubmed/25484425 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.143581 |
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