Introduction: Acute hepatic porphyria (AHP) comprises four rare inherited disorders caused by mutations in genes encoding enzymes of the heme biosynthesis pathway: acute intermittent porphyria (AIP), hereditary coproporphyria (CPOX), variegate porphyria (PPOX), and δ-aminolevulinic acid dehydratase–deficient porphyria (ALAD) (1). Acute intermittent
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