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Motor neuron disease associated with copper deficiency

✍ Scribed by Conrad C. Weihl; Glenn Lopate


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
75 KB
Volume
34
Category
Article
ISSN
0148-639X

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## Abstract A 48‐year‐old man with an IgM plasma cell dyscrasia died after 14 months of symptoms and signs typical of motor neuron disease, including widespread fasciculation and normal sensation. Two laboratory results were atypical: cerebrospinal fluid protein content of 132 mg/dl and slow motor