Summary
A case has been reported in which neuroaxonal dystrophy is present in a patient who had a clinical syndrome compatible with subacute dementia. These findings, accompanied by demyelination and gliosis were restricted to the rostral half of the corpus callosum and the cortical spinal tract. The interrelationship between neuroaxonal dystrophy and dementia is discussed.
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Fujisawa, K.: A unique type of axonal alteration (so-called axonal dystrophy) as seen in Goll's nucleus of 277 cases of controls. A contribution to the pathology of the aging process. Acta neuropath. (Berl.)8, 255–275 (1967).
Jellinger, K., Jirasek, A.: Neuroaxonal dystrophy in man: character and natural history. Acta neuropath. (Berl.) Suppl.V, 3–16 (1971).
Seitelberger, F.: Eine unbekannte Form von infantiler Lipoidspeicher-Krankheit des Gehirns. Proc. 1st Congr. Neuropath., Vol. 3, pp. 323–333. Turin: Rosenberg et Sellier 1952.
—: Neuropathological conditions related to neuroaxonal dystrophy. Acta neuropath. (Berl.) Suppl.V, 17–29 (1971).
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This work was supported in part by Grant Number NB-08549-04 from the National Institute of Neurological Disease and Stroke, Bethesda, Maryland.
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Torack, R.M., Hughes, C.P. Neuroaxonal dystrophy in subacute dementia. Acta Neuropathol 22, 264–268 (1972). https://doi.org/10.1007/BF00684529
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DOI: https://doi.org/10.1007/BF00684529