GENERALIZED GIANT AXONAL NEUROPATHY - CASE WITH FEATURES OF FAZIO-LONDE DISEASE

被引:24
作者
LARBRISSEAU, A
JASMIN, G
HAUSSER, C
BROCHU, P
GEOFFROY, G
机构
[1] ST JUSTINE HOSP CHILDREN,DEPT PATHOL,MONTREAL H3T 1C5,QUEBEC,CANADA
[2] UNIV MONTREAL,MONTREAL 101,QUEBEC,CANADA
来源
NEUROPADIATRIE | 1979年 / 10卷 / 01期
关键词
D O I
10.1055/s-0028-1085316
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The authors present the 8th case so far published of generalized giant axonal neuropathy. Many features of the neurological picture of this 8 year 8 month old boy were suggestive of progressive bulbar paralysis of childhood. Muscle and sural nerve biopsies disclosed typical nodular axonal swellings measuring between 10-29 nm. Ultrastructure of the inflated portions of the axon consisted almost exclusively of 10 nm filaments. Normally appearing constituents were found in the non-dilated portions of the axons with the particularity that glycogen and mitochondria were aggregated. Previous clinical and pathological evidence indicates that this rare disorder not only affects the peripheral nerves but also the whole CNS. This case differs from the others reported in literature by its rapidly deteriorating course and by the prominent involvement of some brain-stem motor functions; a link might be implicated between the entity and Fazio-Londe disease.
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页码:76 / 86
页数:11
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