Neuropathy in Latent Hereditary Hepatic Porphyria

30Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Peripheral nerve conduction velocities were measured in 20 patients with acute intermittent porphyria and five with variegate porphyria and in 25 controls matched for age and sex. None of the porphyric patients had acute symptoms on examination, and nine had never had symptoms. Compared with the controls, patients had a significantly slower conduction velocity of the slower motor fibres of the ulnar nerve (P <0 001) and a slower sensory conduction velocity of the ulnar and median nerves (P<0 05). There was no significant difference between the patients and controls in the maximum motor conduction velocity of the median, ulnar, deep peroneal, or posterior tibial nerves. Slight peripheral neuropathy seems to be associated with latent hereditary hepatic porphyria, even in patients who have never had symptoms. © 1975, British Medical Journal Publishing Group. All rights reserved.

Cite

CITATION STYLE

APA

Mustajoki, P., & Seppalainen, A. M. (1975). Neuropathy in Latent Hereditary Hepatic Porphyria. British Medical Journal, 2(5966), 310–312. https://doi.org/10.1136/bmj.2.5966.310

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free