Lack of cold sensitivity in hyperkalemic periodic paralysis
- 13 October 1986
- journal article
- research article
- Published by Wiley in Muscle & Nerve
- Vol. 9 (8) , 700-703
- https://doi.org/10.1002/mus.880090804
Abstract
The nosologic distinction between paramyotonia congenita and hyperkalemic periodic paralysis is somewhat blurred. Muscle membrane inexcitability induced by cooling seems to be characteristics of paramyotonia congenita. The effect of cooling on the maximal compound muscle action potential (CMAP) in patients with paramyotonia congenita was compared to that in patients with hyperkalemic periodic paralysis. Diminution in CMAP amplitude and area, which was observed in paramyotonia congenita, did not occur in hyperkalemic periodic paralysis. We suggest that this effect of cooling on the CMAP can be utilized in the differentiation of these two syndromes.This publication has 19 references indexed in Scilit:
- Letters to the editorMuscle & Nerve, 1984
- Distinguishing paramyotonia congenita and myotonia congenita by electromyographyMuscle & Nerve, 1983
- Periodic paralysis and the sodium‐potassium pumpAnnals of Neurology, 1982
- Clinical study of paramyotonia congenita with and without myotonia in a warm environmentMuscle & Nerve, 1981
- PARAMYOTONIA CONGENITA: A CLINICAL, HISTOCHEMICAL AND PATHOLOGICAL STUDYBrain, 1972
- ADYNAMIA EPISODICA HEREDITARTABrain, 1969
- The nature of the electrophysiological disorder in adynamia episodica.Journal of Neurology, Neurosurgery & Psychiatry, 1968
- ADYNAMIA EPISODICA HEREDITARIA AND ITS TREATMENTBrain, 1962
- A VARIETY OF PARAMYOTONIA CONGENITAJournal of Neurology, Neurosurgery & Psychiatry, 1957
- Adynamia Episodica HereditariaActa Paediatrica, 1956