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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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Detalles Bibliográficos
Autores principales:	Scurr, Cosmo, Sampson, Barry, Ball, Joanna, Gabriel, Carolyn
Formato:	Texto
Lenguaje:	English
Publicado:	Cases Network Ltd 2009
Materias:	Case report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2769269/ https://www.ncbi.nlm.nih.gov/pubmed/19918559 http://dx.doi.org/10.4076/1757-1626-2-6168

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