PT  - JOURNAL ARTICLE
AU  - Albayram, Sait
AU  - Murphy, Kieran J.
AU  - Gailloud, Philippe
AU  - Moghekar, Abhay
AU  - Brunberg, James A.
TI  - CT Findings in the Infantile Form of Citrullinemia
DP  - 2002 Feb 01
TA  - American Journal of Neuroradiology
PG  - 334--336
VI  - 23
IP  - 2
4099  - http://www.ajnr.org/content/23/2/334.short
4100  - http://www.ajnr.org/content/23/2/334.full
SO  - Am. J. Neuroradiol.2002 Feb 01; 23
AB  - Summary: Citrullinemia is a rare autosomal recessive inborn 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.