Martinez A C, Ferrer M T, Fueyo E, Galdos L
J Neurol Neurosurg Psychiatry. 1975 Feb;38(2):169-74. doi: 10.1136/jnnp.38.2.169.
A case of infantile metachromatic leucodystrophy is described in which symptoms started at 1 year of age with weakness and hypotonus in the lower extremities. The electrophysiological status was typical of a polyneuropathy, showing fibrillation and a reduction of the nerve conduction velocity to 30 percent of the average for normal children of the same age. Clinical signs of a central lesion and mental regression were not evident until a year later. Nerve biopsy showed metachromatic granules in the phagocytes and in the Schwann cells, confirming the diagnosis of metachromatic leucodystrophy. In peripheral neuropathy in infancy without obvious cause, a nerve biopsy is the most appropriate method for diagnosis of the metachromatic leucodystrophy.
本文描述了一例婴儿异染性脑白质营养不良病例,患儿1岁起病,表现为下肢无力和肌张力减退。电生理检查结果为典型的多发性神经病,显示有纤颤,神经传导速度降至同年龄正常儿童平均值的30%。直到一年后才出现中枢病变和智力衰退的临床体征。神经活检显示吞噬细胞和施万细胞中有异染颗粒,确诊为异染性脑白质营养不良。对于无明显病因的婴儿期周围神经病,神经活检是诊断异染性脑白质营养不良的最合适方法。