Diagnosis of Hallervorden-Spatz Disease

J Gordon Millichap

doi:10.15844/pedneurbriefs-9-11-7

Diagnosis of Hallervorden-Spatz Disease

Pediatric Neurology Briefs

Volume 9 (1995): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1995

Abstract

The in vivo diagnosis of Hallervorden-Spatz disease is discussed in relation to the clinical manifestations and MRI findings in two children examined at the Department of Paediatrics, University Hospital of Aarhus, Denmark.

References

Ostergaard JR Christensen T Hansen KN In vivo diagnosis of Hallervorden-Spatz disease Dev Med Child Neurol 1995 Sep 37 9 827 833 10.1111/j.1469-8749.1995.tb12066.x 7589865
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Swisher CN Prensky AL Devivo DE Co-existence of Hallervorden-Spatz disease with acanthocytosis Trans Am Neurol Assoc 1972 97 212 214
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-9-11-7 | Journal eISSN: 2166-6482

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Language: English

Page range: 85 - 85

Published on: Nov 1, 1995

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Diagnosis of Hallervorden-Spatz Disease,

Corticospinal Tract Signs,

Neurodegenerative Disorders

© 1995 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 9 (1995): Issue 11