Two hypothyroid patients, one with autoimmune thyroiditis and pernicious anemia and the other with idiopathic primary myxedema, were studied electrophysiologically. The former showed findings of the Eaton-Lambert myasthenic syndrome, and the latter showed findings of the desensitization block of neuromuscular transmission or the conduction block at the fine terminal filaments of the motor axon. The muscle contraction study revealed the posttetanic muscle contracture without electrical discharges in the former, and the posttetanic twitch depression and the decreased tetanic force in the latter.(26: [326][327][328][329][330][331][332][333][334][335] 1972) S: )INCE the report of Feinberg et al,1 the association of myasthenia gravis and hypo¬ thyroidism has been known, although rela¬ tively infrequent as compared with its as¬ sociation with hyperthyroidism.2 To our knowledge, some of the reported myasthénie patients with hypothyroidism were not nec¬ essarily well-controlled by anticholinesterase drugs.3 7 Norris5 described three patients whose electrophysiological characteristics were not similar to those of myasthenia gravis and were termed "myasthénie syn¬ drome with poor response to edrophonium" by Pearce and Aziz.8 We report two hypothyroid patients with myasthénie syndrome the electrophysiological features of which were different from those of myasthenia gravis. The one represented the Eaton-Lam¬ bert myasthénie syndrome due to a defect of acetylcholine release from the nerve termi¬ nal in association with the findings suggesting autoimmune disturbance, and the other was suggestive of the neuromuscular transmis¬ sion defect due to a desensitization of the postjunctional receptor to acetylcholine or the conduction block at terminal branching points of the motor axon. Abnormalities of the muscle contraction were also investigat¬ ed by determining the posttetanic change of isometric twitches and the tetanus develop¬ ment. The results of electrophysiological studies in these two patients were then com¬ pared with those of 20 normal subjects, 23 patients with myasthenia gravis, and 4 pa¬ tients with Eaton-Lambert myasthénie syn¬ drome associated with bronchogenic carci¬ noma.