Objective. To assess signs of distal neuropathy in patients with acute inte
rmittent porphyria (AIP).
Design. A population-based study.
Subjects. All patients with DNA-verified AIP greater than or equal to 18 ye
ars of age in the four most northerly counties of Sweden.
Intervention. Validated neuropathic signs and tests such as monofilament te
st, neuropathic pain, dry feet, extensor digitorum brevis (EDB) test, loss
of forefoot arch, hammer toes and ulceration.
Results. A total of 356 patients were registered and 339 of them (95%) part
icipated in the neuropathy study. The chronic neurological signs were symme
trical and similar to those in type 1 diabetic patients. Significant impair
ment was found concerning perception, EDB test, lower leg pain, ankle and k
nee tendon reflexes, but not concerning dry feet, loss of forefoot arch and
hammer toes, on comparing patients with manifest versus latent AIP. The ne
urological signs were more severe in the diabetic patients (n = 298). Five
AIP patients had permanent quadriplegia after severe attacks.
Conclusions. Patients with manifest AIP had significantly more signs of dis
tal chronic, symmetrical neuropathy of axonal type than did patients with l
atent AIP. More grave neurological lesions appear to develop after severe a
ttacks.