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The level and features of fatigue development in patients with myasthenia gravis remain not well studied, but their research is promising in order to improve the therapeutic tactics, social, domestic, professional adaptation and, as a consequence, the quality of life of patients in general. The purpose of this work was to quantify the fatigue parameters in patients with myasthenia gravis depending on the form and class of the disease, as well as on the immunological type of the disease. Object and methods. 182 patients with myasthenia were examined (147 (80.8%) patients with a generalized form of the disease, 35 (19.2%) with ocular form). Clinical and neurological examination included complaints collection, history of disease and life, neurological examination. To evaluate the clinical form of myasthenia, the MGFA classification was used. For a quantitative assessment of fatigue, the Fatigue Severity Scale (FSS) was used. The assessment of the level of antibodies to acetylcholine receptors (AchR) and muscle-specific tyrosine kinase (MuSK) by ELISA was performed to all patients, as well as determination of antibodies to titin and SOX1 by indirect immunofluorescence method. In mathematical processing of data, methods of parametric and nonparametric statistics were used. Results and discussion. Among the surveyed patients by gender, women predominated 128 (70.3%), the number of men was 54 (29.7%), the ratio of women to men 2.37:1. Antibodies to acetylcholine receptors were detected in 68.1% of the patients in the general sample (in 73.5% patients with generalized form and in 45.7% - with an ocular form). Antibodies to muscle-specific tyrosine-kinase were detected in 16% of the total number of patients. These antibodies were not detected in patients with ocular myasthenia. Antibodies to titin were detected in almost a third of all subjects - 53 (29.1%). These antibodies were not detected in patients with ocular form of myasthenia gravis. Antibodies to SOX1 were not detected in patients with ocular myasthenia, but diagnosed in 5.5% patients with generalized form. The level of fatigue in patients increases with the increase of the MGFA class of the disease. The median fatigue rate in the general sample corresponded to a mild fatigue level (FSS:36- 44 points), and in patients with generalized myasthenia, it was consistent with moderate fatigue (FSS: 45-53 points). In patients with ocular myasthenia, median fatigue was significantly lower in comparison with the general sample and with the generalized form and did not reach the clinical value (p 0,05; ? = 0,08; p> 0,05, respectively), as well as the presence of antibodies to SOX1 (? = 0.06; p> 0.05). Fatigue significantly correlated with the clinical form of myasthenia (generalized) (? = -0,55; p