KMID : 0359719920100030407
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Journal of the Korean Neurological Association 1992 Volume.10 No. 3 p.407 ~ p.412
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A Case of Suspected Hallervorden-Spatz Disease
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Abstract
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Hallervorden-Spatz discase is a rare, autosomal recessive disorder of mainly early childhood which is chracterized by pigmentary degeneration of the globus pallidus, substantia nigra, and red nucleus. Clinically it manifests various symptoms and
signs
of extrapyramidal and pyramidal involvement.
Authors report a 28-year-old female patient with suspected Hallervorden-Spatz disease in the aspects of clinical and MRI findings suggesting metal deposition in the globus pallidus, substantia nigra, and red nucleus in both side.
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KEYWORD
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