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Porphyria is a rare disease, mostly caused by genetic defects that result in a lack of enzymes involved in the heme synthesis pathway leading to disordered porphyrin metabolism. The clinical manifestations mainly include photosensitive skin damage, abdominal pain, neurological and psychiatric symptoms, and increased blood pressure. According to the site of porphyrin metabolism disorder, it can be divided into erythropoietic porphyria and hepatic porphyria.