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Case Reports
. 2018 Dec;24(12):1305-1308.
doi: 10.1111/cns.13038. Epub 2018 Aug 13.

Motor neuron disease-like phenotype associated with anti-IgLON5 disease

Qing-Qing Tao  1 , Qiao Wei  1 , Shui-Jiang Song  1 , Xin-Zhen Yin  1
Affiliations
Case Reports

Motor neuron disease-like phenotype associated with anti-IgLON5 disease

Qing-Qing Tao et al. CNS Neurosci Ther. 2018 Dec.
No abstract available

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Clinical findings in the patient with anti‐IgLON5 disease. Rapidly progressed intrinsic hand muscle atrophy (A‐B); Brian MRI showed no abnormal signals nor atrophy (C‐F)
See this image and copyright information in PMC

References

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    1. Gaig C, Graus F, Compta Y, et al. Clinical manifestations of the anti‐IgLON5 disease. Neurology. 2017;88(18):1736‐1743. - PMC - PubMed
    1. Sabater L, Gaig C, Gelpi E, et al. A novel non‐rapid‐eye movement and rapid‐eye‐movement parasomnia with sleep breathing disorder associated with antibodies to IgLON5: a case series, characterisation of the antigen, and post‐mortem study. Lancet Neurol. 2014;13(6):575‐586. - PMC - PubMed
    1. Haitao R, Yingmai Y, Yan H, et al. Chorea and parkinsonism associated with autoantibodies to IgLON5 and responsive to immunotherapy. J Neuroimmunol. 2016;300:9‐10. - PubMed
    1. Zhu L, Liu L, Cui S, et al. One case of anti‐IgLON5 syndrome. Chin J Neurol. 2017;10:763‐765.

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