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Copper deficiency myeloneuropathy in a patient with haemachromatosis: a case report
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 r...
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| Main Authors: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Cases Network Ltd
2009
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2769269/ https://ncbi.nlm.nih.gov/pubmed/19918559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4076/1757-1626-2-6168 |
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