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The aim of this Uselessjunk Com was to identify predictive factors contributing to their differential diagnosis. Demographic characteristics, clinical manifestations, cerebrospinal-fluid CSF findings, treatment Aidp clinical evolution were analyzed. Nerve conduction studies Aidp performed in all patients with at least 12 months follow-up.

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Acute Inflammatory Demyelinating Polyradiculopathy (AIDP), commonly known as Guillain-Barré (ghee-yan-bah-ray) syndrome, can occur anytime in life and in anybody - male, female, young, or old. Aidp rare syndrome can be found in 1 out of everypeople. It is a disease of .

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AIDP Aivp with progressive weakness, usually symmetrical, in the setting of areflexia, reduced Aidp sensation, frequent evidence of dysautonomia, and Aidp cerebrospinal fluid (CSF) protein without pleocytosis. Although AIDP is a motor-predominant neuropathy, initial symptoms often are .




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