E-viri
Recenzirano
-
Serrano Russi, A.; Donoghue, S.; Boneh, A.; Manara, R.; Burlina, A.B.; Burlina, A.P.
Molecular genetics and metabolism, November 2018, 2018-11-00, 20181101, Letnik: 125, Številka: 3Journal Article
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.
