CT findings in the infantile form of citrullinemia

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

CT findings in the infantile form of citrullinemia

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

School of Medicine

Research output: Contribution to journal › Article › peer-review

9 Scopus citations

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 language	English (US)
Pages (from-to)	334-336
Number of pages	3
Journal	American Journal of Neuroradiology
Volume	23
Issue number	2
State	Published - 2002

ASJC Scopus subject areas

Radiology Nuclear Medicine and imaging
Clinical Neurology

Cite this

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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.",

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AU - Albayram, Sait

AU - Murphy, Kieran J.

AU - Gailloud, Philippe

AU - Moghekar, Abhay

AU - Brunberg, James A.

PY - 2002

Y1 - 2002

N2 - 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.

AB - 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.

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ER -

CT findings in the infantile form of citrullinemia

Abstract

ASJC Scopus subject areas

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