Concept information
Término preferido
Paralysis, Hyperkalemic Periodic
Notice: Undefined index: in /var/www/html/model/Concept.php on line 545
Tipo
-
mesh:Descriptor
Definición
- An autosomal dominant familial disorder which presents in infancy or childhood and is characterized by episodes of weakness associated with hyperkalemia. During attacks, muscles of the lower extremities are initially affected, followed by the lower trunk and arms. Episodes last from 15-60 minutes and typically occur after a period of rest following exercise. A defect in skeletal muscle sodium channels has been identified as the cause of this condition. Normokalemic periodic paralysis is a closely related disorder marked by a lack of alterations in potassium levels during attacks of weakness. (Adams et al., Principles of Neurology, 6th ed, p1481)
Concepto genérico
Etiquetas alternativas
- Adynamia Episodica Hereditaria
- Adynamia Episodica Hereditaria with or without Myotonia
- Familial Hyperkalemic Periodic Paralysis
- Gamstorp Disease
- Gamstorp Episodic Adynamy
- Hyperkalemic Periodic Paralysis
- Hyperkalemic Periodic Paralysis, Familial
- HyperKPP
- HyperPP
- Myotonic Periodic Paralysis
- Paralysis, Periodic, Hyperkalemic, Familial
- Primary Hyperkalemic Periodic Paralysis
- Sodium Channel Muscle Disease
En otras lenguas
-
francés
-
Adynamie épisodique de Gamstorp
-
Adynamie épisodique héréditaire
-
Maladie de Gamstorp
-
Paralysie périodique familiale hyperkaliémique
URI
http://data.loterre.fr/ark:/67375/JVR-HRL71MBQ-X
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}