Neuropediatrics 1979; 10(1): 76-86
DOI: 10.1055/s-0028-1085316
Case report

© 1979 by Thieme Medical Publishers, Inc.

Generalized Giant Axonal Neuropathy – A Case with Features of Fazio-Londe Disease[1]

A. Larbrisseau, G. Jasmin, C. Hausser, P. Brochu, G. Geoffroy
  • Division of Neurology, Department of Paediatrics and Department of Pathology, Sainte-Justine Hospital for Children and University of Montreal
Further Information

Publication History

1978

1978

Publication Date:
18 November 2008 (online)

We 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 this 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. Our case differs from the others reported in literature by its rapidly deteriorating course and by the prominent involvement of some brain-stem motor functions; we offer the theory that a link might be implicated between this entity and Fazio-Londe disease.

1 Supported in part by the Muscular Dystrophy Association of Canada.

1 Supported in part by the Muscular Dystrophy Association of Canada.

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