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Mol Genet Metab ; 125(3): 276-280, 2018 11.
Article in English | MEDLINE | ID: mdl-30217722

ABSTRACT

Three young patients with glutaric aciduria type I (age 6-23 years) of different ethnic origins, treated for their metabolic disease since early childhood, presented with malignant central nervous system tumors. We recommend continuing clinical follow-up, including monitoring of neurological manifestations and neuroradiological findings, in all patients with glutaric aciduria type I beyond early childhood, especially if adherence to diet is poor or the treatment was not started neonatally.


Subject(s)
Amino Acid Metabolism, Inborn Errors/genetics , Brain Diseases, Metabolic/genetics , Brain Neoplasms/genetics , Brain/metabolism , Glioblastoma/genetics , Glutaryl-CoA Dehydrogenase/deficiency , Adult , Amino Acid Metabolism, Inborn Errors/complications , Amino Acid Metabolism, Inborn Errors/diagnostic imaging , Amino Acid Metabolism, Inborn Errors/physiopathology , Brain/diagnostic imaging , Brain/pathology , Brain Diseases, Metabolic/complications , Brain Diseases, Metabolic/diagnostic imaging , Brain Diseases, Metabolic/physiopathology , Brain Neoplasms/complications , Brain Neoplasms/diagnostic imaging , Brain Neoplasms/physiopathology , Child , Child, Preschool , Female , Glioblastoma/complications , Glioblastoma/diagnostic imaging , Glioblastoma/pathology , Glutarates/metabolism , Glutaryl-CoA Dehydrogenase/genetics , Humans , Male , Young Adult
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