Vol 10: Myasthenia in Acquired Neuromyotonia.Reportar como inadecuado



 Vol 10: Myasthenia in Acquired Neuromyotonia.


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This article is from Journal of Clinical Neurology Seoul, Korea, volume 10.AbstractBackground: Acquired neuromyotonia NMT forms part of the spectrum of acquired peripheral nerve hyperexcitability syndrome, and is thought to be caused by antibodies to voltage-gated potassium channels VGKC. Exertional weakness is unusual unless autoimmune myasthenia gravis MG is superimposed. Case Report: A case of acquired NMT accompanied by exertional weakness without coexistence of seropositive MG is reported herein. Conclusions: Clinical and electrophysiological observations suggest that the cholinergic overactivity in NMT can compromise the safety factor sufficiently to cause a defect in neuromuscular junction transmission.



Autor: Byun, Jung-Ick; Moon, Hye-Jin; Hong, Yoon-Ho

Fuente: https://archive.org/



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