Journal article

Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing

Alice Rudd, Janine Grant, George Varigos, Vanessa Morgan, Ingrid Winship

AUSTRALASIAN JOURNAL OF DERMATOLOGY | WILEY-BLACKWELL | Published : 2013

Abstract

The porphyrias are a group of inherited disorders that result in defects in the enzymes of the haem biosynthetic pathway, causing photosensitive bullous skin eruptions or abdominal and neurological attacks. Enzymatic defects result in specific porphyrin excretory patterns that are diagnosed biochemically and can be confirmed by genetic testing. Defects in the coproporphyrinogen oxidase (CPOX) enzyme result in the autosomal dominant hereditary coproporphyria. Multiple mutations have been identified in the CPOX gene and incomplete penetrance is noted. Latent carriers without clinical evidence of disease are at risk of life-threatening attacks. Porphyria cutanea tarda may be inherited, but is m..

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