Hallervorden-Spatz Disease: Clinicopathology

Abstract

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.

Keywords

• hallervorden-spatz disease
• pathological features
• pallidal axonal spheroids