CT findings in the infantile form of citrullinemia

Sait Albayram, Kieran J. Murphy, Philippe Gailloud, Abhay R Moghekar, James A. Brunberg

Research output: Contribution to journalArticle

Abstract

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 languageEnglish (US)
Pages (from-to)334-336
Number of pages3
JournalAmerican Journal of Neuroradiology
Volume23
Issue number2
StatePublished - 2002

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Citrullinemia
Atrophy
Gyrus Cinguli
Frontal Lobe
Temporal Lobe
Urea

ASJC Scopus subject areas

  • Clinical Neurology
  • Radiology Nuclear Medicine and imaging
  • Radiological and Ultrasound Technology

Cite this

CT findings in the infantile form of citrullinemia. / Albayram, Sait; Murphy, Kieran J.; Gailloud, Philippe; Moghekar, Abhay R; Brunberg, James A.

In: American Journal of Neuroradiology, Vol. 23, No. 2, 2002, p. 334-336.

Research output: Contribution to journalArticle

Albayram, S, Murphy, KJ, Gailloud, P, Moghekar, AR & Brunberg, JA 2002, 'CT findings in the infantile form of citrullinemia', American Journal of Neuroradiology, vol. 23, no. 2, pp. 334-336.
Albayram, Sait ; Murphy, Kieran J. ; Gailloud, Philippe ; Moghekar, Abhay R ; Brunberg, James A. / CT findings in the infantile form of citrullinemia. In: American Journal of Neuroradiology. 2002 ; Vol. 23, No. 2. pp. 334-336.
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