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Published on: July 14, 2016
Episodic hyperCKaemia may be a feature of α-methylacyl-coenzyme A racemase deficiency
B Krett1, V Straub2, J Vissing1
1Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Abstract:
α-methylacyl-CoA racemase (AMACR) deficiency is a rare disorder, affecting peroxisomal metabolism of pristanic acid, with ten published adult cases. We describe an AMACR deficiency case with a clinical presentation dominated by episodic hyperCKaemia, suggesting that myopathic features of AMACR should be considered.
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