Dystonia and Infantile Glutaric Acidemia

J Gordon Millichap

doi:10.15844/pedneurbriefs-3-1-5

Dystonia and Infantile Glutaric Acidemia

Pediatric Neurology Briefs

Volume 3 (1989): Issue 1

By: J Gordon Millichap

Open Access

|Jan 1989

Abstract

Glutaric acidemia, an autosomal recessively inherited disease caused by deficiency of glutaryl-CoA dehydrogenase, was manifested by acute dystonia in 3 infants reported from the Children's Hospital of Pittsburgh, Pennsylvania.

References

Bergman I Finegold D Gartner JC Jr Zitelli BJ Claassen D Scarano J Acute profound dystonia in infants with glutaric acidemia Pediatrics 1989 Feb 83 2 228 234 2643800
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Goodman SI Markey SP Moe PG Miles BS Teng CC Glutaric aciduria; a “new” disorder of amino acid metabolism Biochem Med 1975 Jan 12 1 12 21 10.1016/0006-2944(75)90091-5 1137568
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Kyllerman M Steen G Glutaric aciduria. A “common” metabolic disorder? Arch Fr Pediatr 1980 Apr 37 4 279 7406647
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-3-1-5 | Journal eISSN: 2166-6482

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Language: English

Page range: 4 - 4

Published on: Jan 1, 1989

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Acute Dystonia,

Cerebellar Atrophy,

Temporal Lobes

© 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 1