PURPOSE To identify a pattern of findings on CT or MR of the brain in glutaric acidemia type
I typical enough to permit a correct diagnosis. METHODS Clinical history and findings and …

Rationale and Objectives: In glutaric acidemia type I (GA I), a pediatric neurometabolic
disease that may be mistaken for nonaccidental trauma, expeditious detection is critical as …

Serial CT findings in an infant with glutaric aciduria type I (GA-I) are reported. The major CT
features were dilatation of the insular cisterns, regression of the temporal lobes, with “bat …

Background. Glutaric aciduria type I (GA-I) is a rare inherited metabolic disease with
increased excretion of glutaric acid and its metabolites. Diagnosis is often delayed until the …

Objective To review the imaging features of glutaric aciduria type 1 (GA-1) in a group of 20
patients, the largest published series to date. To document the findings not previously …

We report clinical and neuropathological studies of 2 patients with glutaric aciduria type 1. A
10-month-old male with involuntary movements expired suddenly at home. The second, a …

Glutaric aciduria type I is an uncommon inborn error of metabolism. It is a serious disease,
often with a fatal outcome. This study reports the presence of bilateral temporal fluid …

The neuropathology in three cases of glutaric acidaemia type 1 is presented. All three
showed extensive neuronal loss in the caudate nucleus and the putamen, with only small …

International Perspective Page 1 Glutaric Aciduria Type II: Observations in Seven Patients With
Neonatal- and Late-Onset Disease Mohammed A. Al-Essa, MD Mohamed S. Rashed, PhD …

The case of a 9-month-old girl with glutaric aciduria type 1 (GA 1) is reported. On initial
presentation at 6 months of age, the patient demonstrated bilateral subdural hemorrhages …