Nelson F W, Goldie W D, Hecht J T, Butler I J, Scott C I
Neurology. 1984 Aug;34(8):1053-8. doi: 10.1212/wnl.34.8.1053.
Twenty-three patients with achondroplasia were evaluated using short-latency somatosensory evoked potentials (SEPs) of median and peroneal nerves. Abnormal studies were found in 61%. All patients with neurologic signs or symptoms had abnormal SEPs, with good correlation between SEP results and the level of the lesion determined clinically and radiographically. SEPs were abnormal in 44% of neurologically intact achondroplasts, several of whom had CTs confirming significant foramen magnum stenosis. SEPs are an important noninvasive means of evaluating patients with achondroplasia and are particularly valuable in children to document neurologic compromise before significant and perhaps irreversible clinical impairment develops.
对23例软骨发育不全患者使用正中神经和腓总神经的短潜伏期体感诱发电位(SEP)进行评估。61%的检查结果异常。所有有神经体征或症状的患者SEP均异常,SEP结果与临床及影像学确定的病变程度之间具有良好的相关性。在神经功能正常的软骨发育不全患者中,44%的SEP异常,其中几例患者的CT证实存在明显的枕大孔狭窄。SEP是评估软骨发育不全患者的一种重要的非侵入性方法,对于儿童尤其有价值,可在出现明显且可能不可逆转的临床损害之前记录神经功能损害情况。