Periodic paralysis (Q41414): Difference between revisions
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Grupo raro de transtornos neuromusculares associados a defeitos nos canais iônicos. Caracterizada por episódios intermitentes de fraqueza grave dos membros, geralmente após exercícios pesados, jejum ou refeições ricas em carboidratos. Os três principais tipos de paralisia periódica hereditária incluem paralisia periódica hipocalêmica, paralisia periódica hipercalêmica e síndrome de Andersen-Tawil. | |||
| description / en | description / en | ||
Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or high carbohydrate meals. The three major types of inherited periodic paralysis include hypokalemic periodic paralysis, hyperkalemic periodic paralysis, and Andersen–Tawil syndrome. | |||
Revision as of 07:34, 13 August 2026
Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or high carbohydrate meals. The three major types of inherited periodic paralysis include hypokalemic periodic paralysis, hyperkalemic periodic paralysis, and Andersen–Tawil syndrome.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C74.1 |
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| English | Periodic paralysis |
Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or high carbohydrate meals. The three major types of inherited periodic paralysis include hypokalemic periodic paralysis, hyperkalemic periodic paralysis, and Andersen–Tawil syndrome. |
