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Myasthenia gravis and EL myasthenia synd
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I was hoping that someone could help me understand the pathophysiology of myasthenia SYNDROME (Eaton-Lambert) that explain why such patients tend to have a stronger muscular contraction after some physical effort compared to the Myasthenia Gravis patient that has a weakening of muscular contraction.
I do understand the basic pathophysiology of both diseases as well as the weakening as the day goes by for a MG patient but can not comprehend how an EL patient gets a stronger contraction.
any help to decipher this enigma would greatly appreciated!!!








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