ISAACS SYNDROME: A REVIEW

被引:82
作者
Ahmed, Aiesha [1 ]
Simmons, Zachary [1 ,2 ]
机构
[1] Penn State Hershey Med Ctr, Dept Neurol, Hershey, PA 17033 USA
[2] Penn State Hershey Med Ctr, Dept Humanities, Hershey, PA 17033 USA
关键词
autoimmune disorders; Isaacs syndrome; neuromyotonia; paraneoplastic disorders; peripheral nerve hyperexcitability; PERIPHERAL-NERVE HYPEREXCITABILITY; POTASSIUM CHANNEL-COMPLEX; RIPPLING MUSCLE DISEASE; CRAMP-FASCICULATION SYNDROME; RECESSIVE AXONAL NEUROPATHY; STIFF PERSON SYNDROME; MORVANS-SYNDROME; ACQUIRED NEUROMYOTONIA; AUTOIMMUNE NEUROMYOTONIA; LIMBIC ENCEPHALITIS;
D O I
10.1002/mus.24632
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Isaacs syndrome is a peripheral nerve hyperexcitability (PNH) syndrome that presents as continuous motor activity. Clinical findings include cramps, fasciculations, and myokymia. Electrodiagnosis plays a key role in diagnosis by demonstrating after-discharges on nerve conduction studies, and fasciculation potentials, myokymic discharges, neuromyotonic discharges, and other types of abnormal spontaneous activity on needle examination. Etiopathogenesis involves the interaction of genetic, autoimmune, and paraneoplastic factors, which requires a broad-ranging evaluation for underlying causes. Initial treatment is symptomatic, but immune therapy is often needed and can be effective. The purpose of this review is to describe the syndrome and its pathogenesis, assist the reader in evaluating patients with suspected Isaacs syndrome and distinguishing it from other disorders of PNH, and suggest an approach to management, including both symptomatic and immunomodulating therapy.
引用
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页码:5 / 12
页数:8
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