Hallervorden-Spatz Disease: Clinicopathology

J Gordon Millichap

doi:10.15844/pedneurbriefs-10-4-10

Hallervorden-Spatz Disease: Clinicopathology

Pediatric Neurology Briefs

Volume 10 (1996): Issue 4

By: J Gordon Millichap

Open Access

|Apr 1996

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.

References

Malandrini A Fabrizi GM Bartalucci P Salvadori C Berti G Sabò C Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis Childs Nerv Syst 1996 Mar 12 3 155 60 10.1007/BF00266820 8697459
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-10-4-10 | Journal eISSN: 2166-6482

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Language: English

Page range: 31 - 31

Published on: Apr 1, 1996

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Hallervorden-Spatz Disease,

Pathological Features,

Pallidal Axonal Spheroids

© 1996 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 10 (1996): Issue 4