Pathogenesis and clinical management of liver damage in porphyrias: Mechanisms and therapeutic approaches

doi:10.4254/wjh.v17.i9.107705

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World Journal of Hepatology

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1948-5182

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Hepatol. Sep 27, 2025; 17(9): 107705
Published online Sep 27, 2025. doi: 10.4254/wjh.v17.i9.107705

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Figure 1 Metabolic pathway of porphyrias and associated disorders: Key enzymes. Intermediates and disease subtypes. ALA: Δ-aminolevulinic acid; AIP: Acute intermittent porphyria; ADP: Δ-aminolevulinic acid dehydratase deficiency porphyria; EPP: Erythropoietic protoporphyria; VP: Variegate porphyria; PCT: Porphyria cutanea tarda; HEP: Hepatoerythropoietic porphyria; HCP: Hereditary coproporphyria. This figure was created using FigDraw (Supplementary material; www.figdraw.com).

Citation: Zeng T, Huang SY, Chen JN, Pang JH, Chong YT, Li XH. Pathogenesis and clinical management of liver damage in porphyrias: Mechanisms and therapeutic approaches. World J Hepatol 2025; 17(9): 107705
URL: https://www.wjgnet.com/1948-5182/full/v17/i9/107705.htm
DOI: https://dx.doi.org/10.4254/wjh.v17.i9.107705

Zeng T, Huang SY, Chen JN, Pang JH, Chong YT, Li XH. Pathogenesis and clinical management of liver damage in porphyrias: Mechanisms and therapeutic approaches. World J Hepatol 2025; 17(9): 107705 [PMID: 41024869 DOI: 10.4254/wjh.v17.i9.107705]

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