Neuropatia Motora Multifocal ou Esclerose Lateral Amiotrófica?

In ALS, weakness usually spreads progressively to other body segments over months, with the onset of muscle atrophy, signs of upper motor neuron involvement, and, in many cases, bulbar or respiratory involvement. In Multifocal Motor Neuropathy, the progression is generally much slower, often over years, remaining restricted to certain nerves or limbs for long periods, without pyramidal signs, and with the possibility of stabilization after treatment with intravenous immunoglobulin. #AmyotrophicLateralSclerosis #ALS #MultifocalMotorNeuropathy #Neuromuscular #Neurology