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Positron Emission Tomography Using 64-Copper as a Tracer for the Study of Copper-Related Disorders
Published on: April 28, 2023
Copper deficiency myeloneuropathy in a patient with haemachromatosis: a case report
Cosmo Scurr1, Barry Sampson, Joanna Ball
1Department of Undergraduate Medicine, Imperial College London, SW7 2AZ, UK. cosmo.scurr@ic.ac.uk
Cases Journal
|November 18, 2009
Abstract:
A 64-year-old British Caucasian man presented with red skin wheals and breathlessness and then developed a progressive neurological syndrome. Investigation revealed hereditary haemachromatosis, porphyria, and a myelodysplastic syndrome. No unifying diagnosis was made, and his neurological symptoms remained unexplained, until further studies revealed an underlying copper deficiency.
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