Citrullinemia is a rare autosomal recessive in-born error of the urea cycle due to a deficiency in argininosuccinic acid synthetase. We present two cases of the infantile form of citrullinemia in which CT revealed bilateral and symmetric corticosubcortical hypoattenuating areas, ulegyric changes, and atrophy in the frontal lobes, as well as atrophy in the gyrus cinguli, insulae, and temporal lobes.
|Original language||English (US)|
|Number of pages||3|
|Journal||American Journal of Neuroradiology|
|State||Published - Mar 2 2002|
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging
- Clinical Neurology