Literature DB >> 15505400

Glutaric aciduria type I: outcome in the Republic of Ireland.

E R Naughten1, P D Mayne, A A Monavari, S I Goodman, G Sulaiman, D T Croke.   

Abstract

Twenty-one patients have been diagnosed with glutaric aciduria type I over a 16-year period in the Republic of Ireland, 11 following clinical presentation and 10 following a high-risk screen. Nineteen have been managed with diet. Eight patients have died, of whom 7 were diagnosed clinically. Six had dystonic and one spastic cerebral palsy. Of the 11 patients who did not have cerebral palsy, 10 were diagnosed following a high-risk screen. Seven of the 11 have no abnormal neurological signs; 6 of the 7 have abnormal CT or MRI findings; and no case of striatal degeneration has occurred during the past 14 years in the high-risk screened group.

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Year:  2004        PMID: 15505400     DOI: 10.1023/B:BOLI.0000045777.82784.74

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  7 in total

1.  Glutaric aciduria; a "new" disorder of amino acid metabolism.

Authors:  S I Goodman; S P Markey; P G Moe; B S Miles; C C Teng
Journal:  Biochem Med       Date:  1975-01

2.  Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.

Authors:  E P Treacy; A Lee-Chong; G Roche; B Lynch; S Ryan; S Goodman
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

3.  Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management.

Authors:  A A Monavari; E R Naughten
Journal:  Arch Dis Child       Date:  2000-01       Impact factor: 3.791

4.  Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada.

Authors:  C R Greenberg; A N Prasad; L A Dilling; J R G Thompson; J C Haworth; B Martin; P Wood-Steiman; L E Seargeant; B Seifert; F A Booth; C Prasad
Journal:  Mol Genet Metab       Date:  2002-01       Impact factor: 4.797

5.  Improved assay of glutaryl-CoA dehydrogenase in cultured cells and liver: application to glutaric aciduria type I.

Authors:  E Christensen
Journal:  Clin Chim Acta       Date:  1983-03-28       Impact factor: 3.786

6.  Type I glutaric aciduria, part 1: natural history of 77 patients.

Authors:  Kevin A Strauss; Erik G Puffenberger; Donna L Robinson; D Holmes Morton
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-08-15       Impact factor: 3.908

7.  Neuroimaging findings in glutaric aciduria type 1.

Authors:  Eilish L Twomey; Eileen R Naughten; Veronica B Donoghue; Stephanie Ryan
Journal:  Pediatr Radiol       Date:  2003-10-08
  7 in total
  22 in total

1.  Diagnosis of glutaric aciduria type 1 by measuring 3-hydroxyglutaric acid in dried urine spots by liquid chromatography tandem mass spectrometry.

Authors:  Osama Y Al-Dirbashi; Stefan Kölker; Dione Ng; Lawrence Fisher; Tony Rupar; Nathalie Lepage; Mohamed S Rashed; Tomofumi Santa; Stephen I Goodman; Michael T Geraghty; Johannes Zschocke; Ernst Christensen; Georg F Hoffmann; Pranesh Chakraborty
Journal:  J Inherit Metab Dis       Date:  2010-10-27       Impact factor: 4.982

Review 2.  Emergency treatment in glutaryl-CoA dehydrogenase deficiency.

Authors:  S Kölker; C R Greenberg; M Lindner; E Müller; E R Naughten; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

3.  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

Review 4.  Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.

Authors:  Nikolas Boy; Chris Mühlhausen; Esther M Maier; Jana Heringer; Birgit Assmann; Peter Burgard; Marjorie Dixon; Sandra Fleissner; Cheryl R Greenberg; Inga Harting; Georg F Hoffmann; Daniela Karall; David M Koeller; Michael B Krawinkel; Jürgen G Okun; Thomas Opladen; Roland Posset; Katja Sahm; Johannes Zschocke; Stefan Kölker
Journal:  J Inherit Metab Dis       Date:  2016-11-16       Impact factor: 4.982

5.  Two Uneventful Pregnancies in a Woman with Glutaric Aciduria Type 1.

Authors:  Karolina M Stepien; Gregory M Pastores; Una Hendroff; Ciara McCormick; Patricia Fitzimons; Naveed Khawaja; Ingrid Borovickova; Eileen P Treacy
Journal:  JIMD Rep       Date:  2018-01-03

6.  Low lysine diet in glutaric aciduria type I--effect on anthropometric and biochemical follow-up parameters.

Authors:  Nikolas Boy; Gisela Haege; Jana Heringer; Birgit Assmann; Chris Mühlhausen; Regina Ensenauer; Esther M Maier; Thomas Lücke; Georg F Hoffmann; Edith Müller; Peter Burgard; Stefan Kölker
Journal:  J Inherit Metab Dis       Date:  2012-09-13       Impact factor: 4.982

7.  Impairment of astrocytic glutaminolysis in glutaric aciduria type I.

Authors:  Shoko Komatsuzaki; Raga Deepthi Ediga; Jürgen G Okun; Stefan Kölker; Sven W Sauer
Journal:  J Inherit Metab Dis       Date:  2017-11-02       Impact factor: 4.982

Review 8.  Neonatal screening for glutaric aciduria type I: strategies to proceed.

Authors:  M Lindner; S Ho; J Fang-Hoffmann; G F Hoffmann; S Kölker
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       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.  Glutaric aciduria type I: outcome following detection by newborn screening.

Authors:  S Bijarnia; V Wiley; K Carpenter; J Christodoulou; C J Ellaway; B Wilcken
Journal:  J Inherit Metab Dis       Date:  2008-08-09       Impact factor: 4.982

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