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Abstract

Late onset familial Hallervorden-Spatz disease: MR findings in two sisters.

P Ambrosetto, R Nonni, A Bacci and G Gobbi
American Journal of Neuroradiology January 1992, 13 (1) 394-396;
P Ambrosetto
Department of Neuroradiology, Medical School, University of Bologna, Italy.
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R Nonni
Department of Neuroradiology, Medical School, University of Bologna, Italy.
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A Bacci
Department of Neuroradiology, Medical School, University of Bologna, Italy.
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G Gobbi
Department of Neuroradiology, Medical School, University of Bologna, Italy.
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Abstract

Two sisters affected by late onset Hallervorden-Spatz disease are described. In both patients, MR showed rings of decreased signal intensity surrounding hyperintense areas that gave a target-like appearance to the globi pallidi, a finding that corresponds with the known pathologic lesions in the disease. MR reflects the metabolic and anatomic evaluation of this disease.

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American Journal of Neuroradiology
Vol. 13, Issue 1
1 Jan 1992
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Late onset familial Hallervorden-Spatz disease: MR findings in two sisters.
P Ambrosetto, R Nonni, A Bacci, G Gobbi
American Journal of Neuroradiology Jan 1992, 13 (1) 394-396;

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Late onset familial Hallervorden-Spatz disease: MR findings in two sisters.
P Ambrosetto, R Nonni, A Bacci, G Gobbi
American Journal of Neuroradiology Jan 1992, 13 (1) 394-396;
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