Potassium-aggravated myotonia (Q103252): Difference between revisions
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A miotonia agravada pelo potássio é uma canalopatia muscular que se apresenta com uma miotonia pura dramaticamente agravada pela ingestão de potássio, com sensibilidade variável ao frio e sem fraqueza episódica. Este grupo inclui três formas: miotonia flutuante, miotonia permanente e miotonia responsiva à acetazolamida. | |||
| description / en | description / en | ||
Potassium-aggravated myotonia is a muscular channelopathy presenting with a pure myotonia dramatically aggravated by potassium ingestion, with variable cold sensitivity and no episodic weakness. This group includes three forms: myotonia fluctuans, myotonia permanens, and acetazolamide-responsive myotonia. | |||
Revision as of 09:01, 17 August 2026
Potassium-aggravated myotonia is a muscular channelopathy presenting with a pure myotonia dramatically aggravated by potassium ingestion, with variable cold sensitivity and no episodic weakness. This group includes three forms: myotonia fluctuans, myotonia permanens, and acetazolamide-responsive myotonia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1707250468 |
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| English | Potassium-aggravated myotonia |
Potassium-aggravated myotonia is a muscular channelopathy presenting with a pure myotonia dramatically aggravated by potassium ingestion, with variable cold sensitivity and no episodic weakness. This group includes three forms: myotonia fluctuans, myotonia permanens, and acetazolamide-responsive myotonia. |
