Semin Liver Dis 1998; 18(1): 33-41
DOI: 10.1055/s-2007-1007138
ORIGINAL ARTICLE

© 1998 by Thieme Medical Publishers, Inc.

Variegate Porphyria

Ralph E. Kirsch, Peter N. Meissner, Richard J. Hift
  • Lennox Eales Porphyria Laboratories, MRC/UCT Liver Research Centre, Department of Medicine, University of Cape Town, Cape Town, South Africa
Further Information

Publication History

Publication Date:
17 March 2008 (online)

ABSTRACT

Variegate porphyria is an autosomal dominant inherited trait resulting in decreased activity of protoporphyrinogen oxidase. It is characterized clinically by photosensitive skin disease and a propensity to acute neuro-visceral crises. The disease is found worldwide but has an exceptionally high frequency in South Africa. The gene for human protoporphyrinogen oxidase has been identified and sequenced, and several mutations in the protoporphyrinogen oxidase gene sequence have been identified. In South Africa, fewer patients now present with acute attacks, leaving a greater proportion with skin disease or asymptomatic disease. Acute attacks of variegate porphyria appear to be less easily provoked and to be milder than those associated with acute intermittent porphyria.