Literature DB >> 11174631

Acute encephalopathy despite early therapy in a patient with homozygosity for E365K in the glutaryl-coenzyme A dehydrogenase gene.

S Kölker1, V T Ramaekers, J Zschocke, G F Hoffmann.   

Abstract

A patient with glutaric aciduria type I had an acute encephalopathic crisis despite early treatment. This report indicates that current therapeutic strategies may be insufficient for some high-risk patients and stresses the demand for new approaches in glutaric aciduria type I.

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Year:  2001        PMID: 11174631     DOI: 10.1067/mpd.2001.110303

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  2 in total

Review 1.  Glutaric aciduria type 1 and neonatal screening: time to proceed--with caution.

Authors:  Andrea Superti-Furga
Journal:  Eur J Pediatr       Date:  2003-10-25       Impact factor: 3.183

Review 2.  Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiency.

Authors:  S Kölker; P Burgard; J G Okun; A Schulze-Bergkamen; B Assmann; C R Greenberg; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

  2 in total

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