Primary cutaneous amyloidosis
MONDO:0015301Cutaneous amyloidosis refers to a variety of skin diseases characterized histologically by the extracellular accumulation of amyloid deposits in the dermis. Rare forms include lichen amyloidosus, X-linked reticulate pigmentary disorder, primary localized cutaneous nodular amyloidosis, and macular amyloidosis.
Also known as: primary localised cutaneous amyloidosis, primary localized cutaneous amyloidosis, PLCA, familial primary localised cutaneous amyloidosis, familial primary localized cutaneous amyloidosis, amyloidosis IX, amyloidosis familial cutaneous lichen, amyloidosis, primary localised cutaneous
8 clinical trials for this condition and its sub-types, 4 tagged with Primary cutaneous amyloidosis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Primary cutaneous amyloidosis
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Lichen amyloidosis 2 trials
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3 sub-types
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Macular amyloidosis 1 trial
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Amyloidosis cutis dyschromia 0 trials
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Nodular cutaneous amyloidosis 0 trials