Association of amyloidosis cutis dyschromica and familial Mediterranean fever
Abstract: 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 ethn...
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Main Authors: | , , , |
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Format: | Book |
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Sociedade Brasileira de Dermatologia,
2017-01-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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