摘要: Our present understanding of the syndromes CIDP and MMN is insufficient to separate them clearly. I believe that simply a multifocal, predominantly motor variant CIDP. Furthermore, highly touted resemblance MND has been exaggerated; these are only superficially similar can readily be distinguished on clinical electrophysiologic grounds. rare but probably more common than initially believed; certainly, literature replete with reports cases. Further studies needed clarify fully relationship between role glycolipid antibodies in other syndromes.