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sporadic porphyria cutanea tarda - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

sporadic porphyria cutanea tarda

MONDO:0008295

Also known as:acquired porphyria cutanea tardaporphyria cutanea tarda type IPCT, 'sporadic' type

Overview

An instance of porphyria cutanea tarda that is acquired during the lifetime of the individual.

GeneticsAutosomal dominant

ResearchLimited published research (7 articles)

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include: Fragile skin, Porphyrinuria, Liver scarring (fibrosis) (hepatic fibrosis), and Hypertrichosis and 3 more.

Organ System	Phenotype Count	Example Features
Skin	3	Fragile skin, Hyperpigmentation of the skin, Eczematoid dermatitis

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for sporadic porphyria cutanea tarda.

7 publications have been identified in PubMed for sporadic porphyria cutanea tarda. Research spans Case Report / Case Series (57%), Review / Meta-Analysis (14%), and Basic Science / Preclinical (14%).

Recent Publications

Robinson S (2026). [PMID: 41539024](https://pubmed.ncbi.nlm.nih.gov/41539024/). *Free Radic Biol Med*. [Basic Science / Preclinical]
Aarsand AK (2025). [PMID: 38940544](https://pubmed.ncbi.nlm.nih.gov/38940544/). *Liver Int*. [Review / Meta-Analysis]
Kim JL (2025). [PMID: 40433503](https://pubmed.ncbi.nlm.nih.gov/40433503/). *EJHaem*. [Case Report / Case Series]
Mendez M (2025). [PMID: 41313100](https://pubmed.ncbi.nlm.nih.gov/41313100/). *Medicina (B Aires)*. [Epidemiology / Natural History]
Dotto PG (2025). [PMID: 40534320](https://pubmed.ncbi.nlm.nih.gov/40534320/). *Clin Genet*. [Case Report / Case Series]

Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 3:10 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:176090

Orphanet

European rare disease database

Orphanet:443057

GARD

Genetic and Rare Diseases Info Center

GARD:17749

Questions for Your Care Team

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sporadic porphyria cutanea tarda

Overview

Clinical Presentation

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Orphanet

GARD

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Questions for Your Care Team

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