进行性腓肌萎缩症（附一家系8例报告）

Peroneal muscular atrophy: report of 8 cases of a genealogical tree

本文报告了一家系８例腓骨肌萎缩症。该家系四代３４人，患病８人（２３．５％），男女各半。７例于１０岁前发病。均符合遗传性运动和感觉性神经病Ⅰ型。其中２例经脊髓碘水造影加ＣＴ扫描发现腰骶部神经根增粗，作者认为本症的脑脊液蛋白增高可能与此有关。

This paper reports 8 patients with peroneal muscular atrophy in a genealogical tree. The incidence was 23.5% in this family. Male and female were equally affected.The clinical manifestation appeared before age of 10 in 7 patients, which conformed to hereditary neuropathy(typeⅠ). Among these patients.2 underwent spinal omnipague radiography and CT-sscan and vealed that the nerve roots at lumbosacral portion were thicken. We consider that there may be a relationship between the increase of protein in cerebrospinal fluid and hypertrophy of nerve roots in such patient.