Jacob Ron, Mandel Hanna, Shehadeh Naim
Department of Pediatrics B, Ruth Rapport Children's Hospital, Rambam Health Care Campus, Technion Faculty of Medicine, Haifa, Israel.
Metabolic Unit, Ruth Rapport Children's Hospital, Rambam Health Care Campus, Technion Faculty of Medicine, Haifa, Israel.
Child Neurol Open. 2015 Oct 6;2(4):2329048X15609606. doi: 10.1177/2329048X15609606. eCollection 2015 Oct-Dec.
X-Linked adrenoleukodystrophy is the most common peroxisomal disorder with different phenotypes among patients carrying the same ABCD1 mutation. There were previously reported associations of X-linked adrenoleukodystrophy with autoimmune disorders. The authors describe Guillain Barré syndrome in a child with X-linked adrenoleukodystrophy. The available evidence does not permit conclusion concerning etiological linkage between the 2 diseases, but it warrants further study.
X连锁肾上腺脑白质营养不良是最常见的过氧化物酶体疾病,在携带相同ABCD1突变的患者中具有不同的表型。此前有报道称X连锁肾上腺脑白质营养不良与自身免疫性疾病有关。作者描述了一名患有X连锁肾上腺脑白质营养不良的儿童出现格林-巴利综合征。现有证据无法得出这两种疾病之间存在病因学联系的结论,但值得进一步研究。