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[14] Hepatic Porphyria(s) with Acute Manifestations ALAD-Deficiency Porphyria (ADP) -aminolevulinic acid dehydratase porphyria (ADP) (OMIM 125270) also known as Doss Porphyria and the rarest of all porphyrias, is a genetic disease triggered by a severe insufficiency of the enzyme -aminolevulinic acid dehydratase (ALAD) (Figure 1A)

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