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- Michael L O'Neill, Frank Kuo, and Gaurav Saigal.
- Department of Radiology, Jackson Memorial Hospital, University of Miami Miller School of Medicine, Miami, FL.
- J Neuroimaging. 2014 Jul 1;24(4):414-7.
AbstractBeta-ketothiolase (BKT) deficiency is a rare autosomal recessive metabolic disorder, which causes episodic severe metabolic acidosis. Average onset of disease is from 6 to 24 months. Imaging findings relating to this entity have rarely been reported. We report a case of a 5-year-old girl with BKT deficiency with isolated focal T2 hyperintensities involving the globi pallidi, which demonstrated restricted diffusion. To our knowledge, these imaging findings have not been previously reported in the setting of BKT deficiency.Copyright © 2012 by the American Society of Neuroimaging.
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