Jang Dae-Hyun, Sung In Young, Ko Tae Sung
Department of Rehabilitation, Incheon St Mary's Hospital, the Catholic University of Korea, Incheon, Korea.
J Child Neurol. 2013 Jan;28(1):132-7. doi: 10.1177/0883073812437425. Epub 2012 Feb 28.
Fukuyama congenital muscular dystrophy is characterized by generalized muscle weakness and disturbances in central nervous system migration. Although this disorder is caused by mutations in the fukutin gene, which encodes a protein associated with the hypoglycosylation of α-dystroglycan, the specific functions of fukutin protein are largely unknown. In addition to being found in muscle and brain, α-dystroglycan is expressed in various other tissues including peripheral nerves, suggesting that deficiencies in fukutin may result in abnormal myelination of peripheral nerves due to the aberrant glycosylation of Schwann cell α-dystroglycan. This report describes a 7-year-old girl with Fukuyama congenital muscular dystrophy and demyelinating peripheral polyneuropathy.
福山型先天性肌营养不良的特征是全身肌肉无力以及中枢神经系统迁移紊乱。尽管这种疾病是由福库汀基因的突变引起的,该基因编码一种与α-肌营养不良聚糖低糖基化相关的蛋白质,但福库汀蛋白的具体功能在很大程度上尚不清楚。除了在肌肉和大脑中发现外,α-肌营养不良聚糖还在包括周围神经在内的各种其他组织中表达,这表明福库汀的缺陷可能由于施万细胞α-肌营养不良聚糖的异常糖基化而导致周围神经髓鞘形成异常。本报告描述了一名患有福山型先天性肌营养不良和脱髓鞘性周围多发性神经病的7岁女孩。