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Up to: Inherited porphyria · Hepatic porphyria
Erythropoietic protoporphyria
A rare congenital metabolic disorder characterized by an inborn error of porphyrin-heme biosynthesis. Signs and symptoms include painful cutaneous photosensitivity leading to blistering and scarring of the exposed skin areas, erythrodontia, red discoloration of urine, hemolytic anemia, and splenomegaly.
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X-linked erythropoietic protoporphyria 10 trials
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Autosomal erythropoietic protoporphyria 0 trials · 3 incl. sub-types Sub-types →