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Isaacs Syndrome

More information in Books or onNLM PubMed
Definition: A rare neuromuscular disorder with onset usually in late childhood or early adulthood, characterized by intermittent or continuous widespread involuntary muscle contractions; FASCICULATION; hyporeflexia; MUSCLE CRAMP; MUSCLE WEAKNESS; HYPERHIDROSIS; TACHYCARDIA; and MYOKYMIA. Involvement of pharyngeal or laryngeal muscles may interfere with speech and breathing. The continuous motor activity persists during sleep and general anesthesia (distinguishing this condition from STIFF-PERSON SYNDROME). Familial and acquired (primarily autoimmune) forms have been reported. (From Ann NY Acad Sci 1998 May 13;841:482-496; Adams et al., Principles of Neurology, 6th ed, p1491)      Other names Syndromes, Isaacs-Mertens; Syndromes, Gamstorp-Wohlfart; Neuromyotonia, Acquired; Myokymias, Continuous; Isaacs Pseudomyotonia Syndrome; Isaacs Mertens Syndrome; Isaac Syndrome; Gamstorp-Wohlfart Syndromes; Gamstorp Wohlfart Syndrome; Continuous Myokymias; Continuous Myokymia; Syndrome of Continuous Muscle Activity; Quantal Squander; Pseudomyotonia Syndrome of Isaacs; Isaacs-Mertens Syndrome; Isaacs' Syndrome; Gamstorp-Wohlfart Syndrome; Continuous Muscle Activity Syndrome; Acquired Neuromyotonia; Pseudomyotonia

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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