Donaghy M, Brett E M, Ormerod I E, King R H, Thomas P K
Department of Neurological Science, Royal Free Hospital School of Medicine, London, UK.
J Neurol Neurosurg Psychiatry. 1988 Jul;51(7):991-4. doi: 10.1136/jnnp.51.7.991.
A further child with giant axonal neuropathy (GAN), abnormally curly hair and consanguineous parents is described. Of the 19 patients with GAN so far reported in the literature, six, including the present patient, have resulted from consanguineous marriages. This makes autosomal recessive inheritance of GAN highly probable. Our patient also exhibited cerebellar ataxia and signs of pyramidal tract damage; magnetic resonance brain imaging demonstrated abnormalities within the cerebellar and cerebral white matter. Myelinated nerve fibre density in the sural nerve was reduced to 6790/mm2 at age 8 years and had fallen to 3812/mm2 16 months later, indicating that progressive axonal loss occurs in GAN.
本文描述了一名患有巨大轴索神经病(GAN)、头发异常卷曲且父母为近亲结婚的儿童。在文献中迄今报道的19例GAN患者中,包括本患者在内有6例源于近亲婚姻。这使得GAN极有可能为常染色体隐性遗传。我们的患者还表现出小脑共济失调和锥体束受损的体征;脑部磁共振成像显示小脑和脑白质存在异常。腓肠神经有髓神经纤维密度在8岁时降至6790/mm²,16个月后降至3812/mm²,表明GAN存在进行性轴索丧失。