Drug treatment in acute porphyria.

  • Abel Gorchein
  • Published 1997 in British journal of clinical pharmacology

Abstract

The acute hepatic porphyrias are rare pharmacogenetic diseases inherited as autosomal dominant conditions of low penetrance. The genetic defect is a 50% deficiency of an enzyme of the haem biosynthetic pathway. Patients may develop 'neurovisceral attacks' which include severe abdominal pain, neuropsychiatric manifestations and potentially fatal respiratory… (More)

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