The various types of acute porphyria are discussed, as well as their mode o
f inheritance and the enzyme deficiencies responsible for the symptoms. The
symptoms and signs of an acute attack are then described, especially those
due to neuropathies and to disturbances of behaviour. Agents which can pre
cipitate attacks are listed. These are most frequently drugs, and as they i
nclude those used for anti-epileptic treatment problems soon arise as seizu
res often occur in this condition. The main complications are hypertension
and renal failure, and examples of hyponatraemia and folate deficiency are
illustrated. The urgency to diagnose this disorder lies in the need to avoi
d precipitating factors. Screening tests are discussed, and those needed to
confirm the diagnosis. The prognosis has improved over the years, due to i
ncreased awareness of the disorder, and better management. During an acute
attack the treatment of pain and vomiting will be of particular importance,
and then haematin or chelating agents can be tried. With better management
most of those who have inherited acute porphyria should be able to lead a
normal life. (C) 1999 Elsevier Science B.V. All rights reserved.