Copper deficiency myeloneuropathy in a patient with haemachromatosis: a case report

نویسندگان

  • Cosmo Scurr
  • Barry Sampson
  • Joanna Ball
  • Carolyn Gabriel
چکیده

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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عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2009