Is it time to start to consider treating the liver in glutaric aciduria type 1?

J Inherit Metab Dis. 2023 Jul;46(4):539-540. doi: 10.1002/jimd.12623. Epub 2023 May 17.

Authors

Sander Houten¹, Curtis R Coughlin 2nd²

Affiliations

¹ Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
² Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.

PMID: 37162343
DOI: 10.1002/jimd.12623

No abstract available

Publication types

Editorial

MeSH terms

Amino Acid Metabolism, Inborn Errors* / genetics
Amino Acid Metabolism, Inborn Errors* / therapy
Brain Diseases, Metabolic*
Glutarates
Glutaryl-CoA Dehydrogenase / deficiency
Humans
Liver

Substances

Glutaryl-CoA Dehydrogenase
Glutarates

Supplementary concepts

Glutaric Acidemia I