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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1980-11-20
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pubmed:abstractText |
The term neuromyotonia has been applied to spontaneous activity of peripheral motor nerves which gives rise to pseudomyotonia, muscular fasciculations and myokymia. A family is described in which 8 members of 3 generations suffer from the spinal form of Charcto-Marie-Tooth disease (distal type of chronic spinal atrophy). 5 of the 8 members were examined and found to have myokymia, accentuated by voluntary muscle contraction. Pseudomyotonia was present in 2 patients and, in the 1 patient treated, was abolished by carbamazepine. The association between neuromyotonia and charcto-Marie-Tooth disease has been reported in only 7 patients before but may be more common than previously thought because muscle cramps are reported to be a feature of this disorder.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0196-6383
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
49-56
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:550956-Adult,
pubmed-meshheading:550956-Aged,
pubmed-meshheading:550956-Carbamazepine,
pubmed-meshheading:550956-Charcot-Marie-Tooth Disease,
pubmed-meshheading:550956-Electromyography,
pubmed-meshheading:550956-Fasciculation,
pubmed-meshheading:550956-Female,
pubmed-meshheading:550956-Humans,
pubmed-meshheading:550956-Male,
pubmed-meshheading:550956-Middle Aged,
pubmed-meshheading:550956-Muscle Contraction,
pubmed-meshheading:550956-Muscular Atrophy,
pubmed-meshheading:550956-Neural Conduction,
pubmed-meshheading:550956-Pedigree,
pubmed-meshheading:550956-Syndrome
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pubmed:year |
1979
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pubmed:articleTitle |
Neuromyotonia in the spinal form of Charcot-Marie-Tooth disease.
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pubmed:publicationType |
Journal Article,
Case Reports
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