Neuroaxonal Dystrophy

J Gordon Millichap

doi:10.15844/pedneurbriefs-3-6-4

Neuroaxonal Dystrophy

Pediatric Neurology Briefs

Volume 3 (1989): Issue 6

By: J Gordon Millichap

Open Access

|Jun 1989

Abstract

The clinical, pathological and biochemical findings in two brothers with a newly recognized form of infantile neuroaxonal dystrophy associated with alpha-N-acetylgalactosaminidase deficiency are reported from the Divisions of Medical and Molecular Genetics and Neuropathology, Mount Sinai School of Medicine, New York; Department of Chemistry, University of Alberta, Edmonton, Canada; Department of Physiological Chemistry, University of Bonn, Federal Republic of Germany; and Department of Hunan Genetics, University of Wurzburg, Federal Republic of Germany.

References

Schindler D Bishop DF Wolfe DE Wang AM Egge H Lemieux RU Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency N Engl J Med 1989 Jun 29 320 26 1735 40 10.1056/NEJM198906293202606 2733734
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Ito M Okuno T Asato R Mutoh K Nakano S Kataoka K MRI in infantile neuroaxonal dystrophy Pediatr Neurol 1989 Jul-Aug 5 4 245 8 10.1016/0887-8994(89)90083-0 2803380
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-3-6-4 | Journal eISSN: 2166-6482

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Language: English

Page range: 43 - 44

Published on: Jun 1, 1989

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Alpha-N-Acetylgalactosaminidase,

Neuroaxonal Dystrophies,

Hallervorden-Spatz Syndrome

© 1989 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 3 (1989): Issue 6