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neuromyotonia

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Also known as Isaacs syndrome, Quantal squander syndrome, Peripheral nerve hyperexcitability, Continuous muscle fiber activity syndrome, Isaac-Mertens syndrome, Acquired neuromyotonia

Neuromyotonia (NMT) is a form of peripheral nerve hyperexcitability that causes spontaneous muscular activity resulting from repetitive motor unit action potentials of peripheral origin. NMT along with Morvan's syndrome are the most severe types in the Peripheral Nerve Hyperexciteability spectrum. Example of two more common and less severe syndromes in the spectrum are cramp fasciculation syndrome and benign fasciculation syndrome. NMT can have both hereditary and acquired (non-inherited) forms. The prevalence of NMT is unknown.

Key facts

Medical condition (new).name
Neuromyotonia
Medical condition (new).synonyms
Isaacs syndrome, Isaacs-Mertens syndrome

via Wikipedia infobox

~8 min read

Encyclopedic overview

8 sections
Contents
  • Signs and symptoms
  • Causes
  • Diagnosis
  • Types
  • Peripheral nerve hyperexcitability
  • Treatments
  • Prognosis
  • References

Neuromyotonia (NMT) is a form of peripheral nerve hyperexcitability that causes spontaneous muscular activity resulting from repetitive motor unit action potentials of peripheral origin. NMT along with Morvan's syndrome are the most severe types in the Peripheral Nerve Hyperexciteability spectrum. Example of two more common and less severe syndromes in the spectrum are cramp fasciculation syndrome and benign fasciculation syndrome. NMT can have both hereditary and acquired (non-inherited) forms. The prevalence of NMT is unknown.

== Signs and symptoms == NMT is a diverse disorder. As a result of muscular hyperactivity, patients may present with muscle cramps, stiffness, myotonia-like symptoms (slow relaxation), associated walking difficulties, hyperhidrosis (excessive sweating), myokymia (quivering of a muscle), fasciculations (muscle twitching), fatigue, exercise intolerance, myoclonic jerks and other related symptoms. These neuromyotonic discharges can cause bursts of spontaneous motor activity that present either continuously or in recurring, decrementing clusters. They can start and stop abruptly, typically waning in strength and are unaffected by voluntary activity.

Excerpted from Wikipedia’s “neuromyotonia” article, available under the CC BY-SA 4.0 licence.