Case report: Isolated muscle neuromyotonia, as presenting feature of Isaacs' syndrome
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DOI: 10.1016/j.jneuroim.2021.577491
Abstract: An autoimmune form of Isaacs' syndrome is commonly associated with VGKC complex antibodies and characterized by continuous muscle activity of extremity muscles. Here, we describe a CASPR2 and LGI1 positive patient with neuromyotonia clinically and… read more here.
Keywords: muscle; isaacs syndrome; neuromyotonia; report isolated ... See more keywords