Abstract
A 21/2 year old girl was admitted to the hospital because of recurrent vomitting, impaired consciousness, and hyperammonemia. MR and CT findings resembled an infarct, but she was found to have a defect in the urea cycle, partial ornithine transcarbamylase deficiency.
References
Filloux F, Townsend JJ, Leonard C (1986) Ornithine transcarbamylase deficiency: neuropathologic changes acquired in utero. J Pediatr 108:942
Kendall BE, Kingsley DP, Leonard JV, Lingam S, Oberholzer VG (1983) Neurological features and computed tomography of the brain in children with ornithine carbamyl transferase deficiency. J Neurol Neurosurg Psychiatry 46:28
Mirowitz SA, Saitor K, Prensky AJ, Gado M, Hodges FJ (1991) Neurodegenerative diseases of childhood: MR and CT evaluation. JCAT 15:210
Msall M, Batshaw ML, Suss R, Brusilow SW, Mellits ED (1984) Neurologic outcome in children with inborn errors of urea synthesis. NEJM 310:1500
Takayanagi M, Ohtake A, Ogura N, Nakajima H, Hoshino M (1984) A female case of ornithine transcarbamylase deficiency with marked computed tomographic abnormalities of the brain. Brain Dev 6:58
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Mamourian, A.C., du Plessis, A. Urea cycle defect: a case with MR and CT findings resembling infarct. Pediatr Radiol 21, 594–595 (1991). https://doi.org/10.1007/BF02012608
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02012608