PCT, the most common type of porphyria, is in most cases (type I) an acquired deficiency of Uroporphyrinogen decarboxylase (UROD), the fifth enzyme in heme biosynthesis, caused by underlying liver diseases triggered by alcohol, iron overload, chlorinated hydrocarbons, oestrogens or viral hepatitis (Frank and Poblete-Gutierrez, 2010). Here, UROD is linked to porphyria cutanea tarda.