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Up to: Hereditary skeletal muscle disorder · Myotonic syndrome · SCN4A-related channelopathy
Paramyotonia congenita of Von Eulenburg
Paramyotonia congenita of Von Eulenburg is characterized by exercise- or cold-induced myotonia and muscle weakness. Prevalence is unknown. The syndrome is nonprogressive and is transmitted as an autosomal dominant trait. It is caused by mutations in the gene encoding the alpha subunit of the type IV voltage-gated sodium channel (SCN4A; 17q23.3).
This condition has no sub-types.