Luijten J A, Straks W, Blikkendaal-Lieftinck L F, Staal G E, Willemse J
Neuropadiatrie. 1978 Nov;9(4):338-50. doi: 10.1055/s-0028-1091493.
The ultrastructural findings in the peripheral nerve of three cases of M. L. D., namely of the late infantile, the juvenile and the adult form are described. The pathological changes consist of two phenomena: segmental demyelination and lysosomal storage of sulfatides, both probably separate results of a deficiency of the enzyme Arylsulfatase A. Some differences are found in the degree of segmental demyelination and the type of lysosomal storage products. A possible relation between these differences and the supposed difference in the defect of the enzyme Arylsulfatase A, responsible for the different subtypes of the disease, is postulated.
描述了三例异染性脑白质营养不良(M.L.D.)患者外周神经的超微结构发现,分别为晚婴型、少年型和成年型。病理变化包括两种现象:节段性脱髓鞘和硫脂在溶酶体中的蓄积,这两者可能都是芳基硫酸酯酶A缺乏的独立结果。在节段性脱髓鞘程度和溶酶体蓄积产物类型方面发现了一些差异。推测了这些差异与假定的负责该疾病不同亚型的芳基硫酸酯酶A缺陷差异之间的可能关系。