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Article

Hereditary coproporphyria.

Seminars in liver disease - 1 Jan 1998

Martásek P

Abstract excerpt

Hereditary coproporphyria (HC) is a rare acute hepatic porphyria. Attacks may be precipitated by certain drugs, alcohol, infections, or low caloric intake. HC is caused by defects in the enzyme coproporphyrinogen III oxidase (copro-ox) which converts coproporphyrinogen III (coprogen) to protoporphyrinogen IX (protogen). Coprogen is made mainly in the liver and is excreted predominantly in the feces. The dramatic...

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PMID: 9516675
DOI: 10.1055/s-2007-1007137

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