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Association of amyloidosis cutis dyschromica and familial Mediterranean fever
Amyloidosis cutis dyschromica is a rare type of primary cutaneous amyloidosis characterized by reticulate hyper-pigmentation with discrete hypopigmented macules. Up to date, about 50 cases of amyloidosis cutis dyschromica have been reported and the majority are familial cases of Asian ethnicity. Var...
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| 發表在: | An Bras Dermatol |
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| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Sociedade Brasileira de Dermatologia
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5726667/ https://ncbi.nlm.nih.gov/pubmed/29267436 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20176114 |
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