CT hypodensity on cerebral white matter in Wilson's disease
Wilson's disease in an autosomal recessive disorder of copper metabolism where systemic manifestations are secondary to thei accumulation of copper in hepatic, nervous and other tissues. In CNS, the structural lesions most commonly found by CT scan are ventricular dilatation, cortical atrophy,...
| Những tác giả chính: | , , , , |
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| Định dạng: | Bài viết |
| Ngôn ngữ: | English |
| Được phát hành: |
Academia Brasileira de Neurologia (ABNEURO)
1991-06-01
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| Loạt: | Arquivos de Neuro-Psiquiatria |
| Truy cập trực tuyến: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1991000200017&lng=en&tlng=en |