An autopsy case of amyotrophic lateral sclerosis with waldenström macroglobulinemia and anti-MAG gammopathy

3Citations
Citations of this article
18Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

We report the case of a 71-year-old woman with typical signs of bulbar amyotrophic lateral sclerosis (ALS) associated with immunoglobulin M (IgM) monoclonal gammopathy and anti-MAG (myelin-associated glycoprotein) antibodies. This unusual association between ALS and anti-MAG antibodies has previously been reported in a single case. Our present case, at neuropathological examination, demonstrated no causative link between anti-MAG antibodies and ALS. © 2011 S. Karger AG, Basel.

Cite

CITATION STYLE

APA

Jurici, S., Laquerrière, A., Bedat-Millet, A. L., Jardin, F., Musset, L., Vallat, J. M., … Martinaud, O. (2011). An autopsy case of amyotrophic lateral sclerosis with waldenström macroglobulinemia and anti-MAG gammopathy. Case Reports in Neurology, 3(3), 294–300. https://doi.org/10.1159/000335004

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free