Literature DB >> 6775244

Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis.

R L Leibel, V E Shih, S I Goodman, M L Bauman, E R McCabe, R G Zwerdling, I Bergman, C Costello.   

Abstract

A boy with glutaric acidemia had psychomotor retardation first noted at age 6 months, recurrent metabolic acidosis, and a progressive quadriparesis with choreoathetosis. He died at age 3 1/2 years. Cultured skin fibroblasts lacked glutaryl-CoA dehydrogenase activity. There was a biochemical, but not a clinical, response to dietary restriction of lysine and tryptophan. The caudate and putamen of the brain showed severe loss of nerve cells and fibers with proliferation of astrocytes, as well as markedly reduced gamma-aminobutyric acid and glutamate decarboxylase activity.

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Year:  1980        PMID: 6775244     DOI: 10.1212/wnl.30.11.1163

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  27 in total

1.  Glutaric aciduria type I: pathomechanisms of neurodegeneration.

Authors:  K Ullrich; B Flott-Rahmel; P Schluff; U Musshoff; A Das; T Lücke; R Steinfeld; E Christensen; C Jakobs; A Ludolph; A Neu; R Röper
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

2.  Inhibition of energy production in vitro by glutaric acid in cerebral cortex of young rats.

Authors:  C G Silva; A R Silva; C Ruschel; C Helegda; A T Wyse; C M Wannmacher; C S Dutra-Filho; M Wajner
Journal:  Metab Brain Dis       Date:  2000-06       Impact factor: 3.584

Review 3.  Challenges for basic research in glutaryl-CoA dehydrogenase deficiency.

Authors:  S Kölker; K A Strauss; S I Goodman; G F Hoffmann; J G Okun; D M Koeller
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

4.  Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

Authors:  S Kölker; E Christensen; J V Leonard; C R Greenberg; A B Burlina; A P Burlina; M Dixon; M Duran; S I Goodman; D M Koeller; E Müller; E R Naughten; E Neumaier-Probst; J G Okun; M Kyllerman; R A Surtees; B Wilcken; G F Hoffmann; P Burgard
Journal:  J Inherit Metab Dis       Date:  2007-01-03       Impact factor: 4.982

5.  Glutaric aciduria type 1: biochemical investigations and postmortem findings.

Authors:  M J Bennett; N Marlow; R J Pollitt; J K Wales
Journal:  Eur J Pediatr       Date:  1986-10       Impact factor: 3.183

Review 6.  The genetics of primary torsion dystonia.

Authors:  U Müller; K G Kupke
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

7.  Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensation.

Authors:  C E Keegan; D M Martin; D J Quint; J L Gorski
Journal:  Eur J Pediatr       Date:  2003-02-07       Impact factor: 3.183

8.  Symptoms and signs in organic acidurias.

Authors:  N J Brandt
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

9.  Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency.

Authors:  S W Sauer
Journal:  J Inherit Metab Dis       Date:  2007-09-21       Impact factor: 4.982

10.  Infantile bilateral striatal necrosis. Clinical and morphological report of a case and a review of the literature.

Authors:  M Röyttä; I Olsson; P Sourander; P Svendsen
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

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