Channelpedia

PubMed 22083238


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Cav1.1 , ClvC1 , ClvC4 , Kir1.1 , Kir2.1 , Nav1.4



Title: Novel Insights into the Pathomechanisms of Skeletal Muscle Channelopathies.

Authors: James A Burge, Michael G Hanna

Journal, date & volume: , 2011 Nov 15 , ,

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22083238


Abstract
The nondystrophic myotonias and primary periodic paralyses are an important group of genetic muscle diseases characterized by dysfunction of ion channels that regulate membrane excitability. Clinical manifestations vary and include myotonia, hyperkalemic and hypokalemic periodic paralysis, progressive myopathy, and cardiac arrhythmias. The severity of myotonia ranges from severe neonatal presentation causing respiratory compromise through to mild later-onset disease. It remains unclear why the frequency of attacks of paralysis varies greatly or why many patients develop a severe permanent fixed myopathy. Recent detailed characterizations of human genetic mutations in voltage-gated muscle sodium (gene: SCN4A), chloride (gene: CLCN1), calcium (gene: CACNA1S), and inward rectifier potassium (genes: KCNJ2, KCNJ18) channels have resulted in new insights into disease mechanisms, clinical phenotypic variation, and therapeutic options.