Literature DB >> 973804

Progressive spastic paraparesis and adrenal insufficiency.

M Gumbinas, H M Liu, G Dawson, M Larsen, O Green.   

Abstract

A 10-year-old boy with progressive paraparesis, personality change, and seizures had laboratory evidence of adrenal insufficiency. Pathologic study showed cerebral edema, but no loss of myelin. Notable pathologic changes were limited to the spinal cord, where the corticospinal and spinocerebellar tracts were demyelinated. Lipid analysis of the brain was normal apart from the finding that galactocerebroside contained a higher proportion than normal of alpha-hydroxy fatty acids. We suggest that this case represents a distinct disease, differing importantly from adrenoleukodystrophy. The underlying defect appears to be in the early enzymatic pathway before cholesterol synthesis, although it is also possible that the defect is at the cell membrane.

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Year:  1976        PMID: 973804     DOI: 10.1001/archneur.1976.00500100012006

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  4 in total

1.  Adrenomyeloneuropathy. A protracted, pseudosystematic variant of adrenoleukodystrophy.

Authors:  A Probst; J Ulrich; P U Heitz; N Herschkowitz
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

2.  A combination of spastic paraparesis, polyneuropathy and adrenocortical insufficiency-a childhood form of adrenomyeloneuropathy.

Authors:  K Toifl; B Mamoli; F Waldhauser
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

3.  Adrenomyeloneuropathy. A report on two families.

Authors:  J J Martin; A Lowenthal; C Ceuterick; H Gacoms
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

4.  Serum cortisol levels of multiple sclerosis patients during ACTH treatment.

Authors:  E Maida; K Summer
Journal:  J Neurol       Date:  1979-03-22       Impact factor: 4.849

  4 in total

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