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潜伏性遗传性肝卟啉症中的神经病变

Neuropathy in latent hereditary hepatic porphyria.

作者信息

Mustajoki P, Seppălăinen A M

出版信息

Br Med J. 1975 May 10;2(5966):310-2. doi: 10.1136/bmj.2.5966.310.

Abstract

Peripheral nerve conduction velocoties 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 less than 0-001) and a slower sensory conduction velocity of the ulnar and median nerves (P less than 0-05). There was no significant difference between the patients and controls in the maximum motor conductionvelocity 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.

摘要

对20例急性间歇性卟啉病患者、5例混合型卟啉病患者以及25名年龄和性别匹配的对照者进行了周围神经传导速度测定。所有卟啉病患者在检查时均无急性症状,其中9例从未出现过症状。与对照组相比,患者尺神经较慢运动纤维的传导速度显著减慢(P<0.001),尺神经和正中神经的感觉传导速度也较慢(P<0.05)。正中神经、尺神经、腓深神经或胫后神经的最大运动传导速度在患者和对照组之间无显著差异。即使是从未出现过症状的患者,轻微的周围神经病变似乎也与潜在的遗传性肝卟啉病有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ee6/1681914/24fa3e1d6dab/brmedj01446-0022-a.jpg

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