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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:
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