Electron microscopic study of skeletal muscle in the Lambert–Eaton myasthenic syndrome

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Abstract

Skeletal muscle biopsies of 7 patients with Lambert–Eaton syndrome were studied. Revealed that specific changes in the neuromuscular junctions are the complication of the postsynaptic region organization. Along with this, there is a destructive process in axon terminals, which may be terminated by the denervation of muscle fibers. Violations of the structure of muscle fibers were observed. A new hypothesis of the Lambert–Eaton syndrome pathogenesis was preposed.

About the authors

L. L. Babakova

The Institute of General Pathology and Pathophysiology, Russian Academy of Medical Sciences, Moscow

Email: fake@neicon.ru
Russian Federation

O. M. Pozdnyakov

The Institute of General Pathology and Pathophysiology, Russian Academy of Medical Sciences, Moscow

Author for correspondence.
Email: opozdnyakov@rambler.ru
Russian Federation

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