Hallervorden-Spatz Disease: Clinicopathology
Clinical and pathological features of familial late infantile Hallervorden-Spatz disease (HSD) are reported in two sisters, one of whom died at 11 years, from the Institute for Neurological Sciences, University of Siena, Italy.
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
1996-04-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/2535 |