The acute porphyrias

Authors
Citation
N. Gordon, The acute porphyrias, BRAIN DEVEL, 21(6), 1999, pp. 373-377
Citations number
20
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
BRAIN & DEVELOPMENT
ISSN journal
03877604 → ACNP
Volume
21
Issue
6
Year of publication
1999
Pages
373 - 377
Database
ISI
SICI code
0387-7604(199909)21:6<373:TAP>2.0.ZU;2-9
Abstract
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.