Debruyne J, Dehaene I, Martin J J
J Neurol Sci. 1980 Sep;47(3):385-94. doi: 10.1016/0022-510x(80)90091-x.
Clinical and neurophysiological studies were carried out in hereditary pressure-sensitive neuropathy. In 4 generations, 19 out of 87 family members were affected. The transmission of the disorder is autosomal dominant with total penetrance but variable expression. The motor conduction velocities of peripheral nerves were slowed even in clinically unaffected nerves. Light- and electron-microscopic studies were performed in the fibular nerve of one patient. A characteristic tomaculous neuropathy was discovered.
对遗传性压力敏感性神经病进行了临床和神经生理学研究。在4代人中,87名家庭成员中有19人患病。该疾病的遗传方式为常染色体显性遗传,完全显性但表现度可变。即使在临床未受影响的神经中,周围神经的运动传导速度也减慢。对一名患者的腓神经进行了光镜和电镜研究。发现了一种典型的腊肠样神经病。