Juvenile metachromatic leucodystrophy

Clicks: 127
ID: 115629
1970
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Abstract
Clinical history, histopathological, ultrastructural and biochemical observations are presented in a juvenile MLD with onset at 8 years and death at 20 years. The findings are compared with related ones in different age groups, and current views on sulfatide metabolism and enzymatic pathogenesis in MLD are briefly entertained. It is postulated that the relatively well established morphological and chemical stability of the nervous tissue at the time of appearance of the metabolic derangement was an important factor in the pathomechanism of the disease process in this particular variant.
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haberland1970actajuvenile Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Catherine Haberland;Eric Brunngraber;Lloyd Witting;Aruna Daniels;Catherine Haberland;Eric Brunngraber;Lloyd Witting;Aruna Daniels;
Journal acta neuropathologica
Year 1970
DOI
doi:10.1007/BF00697745
URL
https://link.springer.com/article/10.1007/BF00697745
Keywords
pathology neurosciences

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