Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
April 1984
in “
Archives of Dermatology
”
Porphyria cutanea tarda skin lesions sun-exposed areas increased fragility vesicles erosions pigmentation changes hypertrichosis sclerodermoid changes scarring alopecia calcification milia uroporphyrinogen decarboxylase deficiency autosomal-dominant inherited form sporadic form hepatocytes RBCs PCT skin fragility skin vesicles skin erosions skin pigmentation changes excessive hair growth skin thickening hair loss with scarring skin calcification skin milia URO-D deficiency inherited form red blood cells
Studysummary This article reviews the characteristics, causes, and types of porphyria cutanea tarda but presents no new findings, focusing instead on existing knowledge about the disorder.
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