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Erythropoietic protoporphyria

Erythropoietic protoporphyria

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3132815979eb492daf2f6a9bee1bb297

Erythropoietic protoporphyria

About this item

Full title

Erythropoietic protoporphyria

Publisher

England: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2009-09, Vol.4 (1), p.19-19, Article 19

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

Erythropoietic protoporphyria (EPP) is an inherited disorder of the haem metabolic pathway characterised by accumulation of protoporphyrin in blood, erythrocytes and tissues, and cutaneous manifestations of photosensitivity. EPP has been reported worldwide, with prevalence between 1:75,000 and 1:200,000. It usually manifests in early infancy upon t...

Alternative Titles

Full title

Erythropoietic protoporphyria

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3132815979eb492daf2f6a9bee1bb297

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3132815979eb492daf2f6a9bee1bb297

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/1750-1172-4-19

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