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Paramyotonia congenita of Von Eulenburg
rareParamyotonia 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).
- Identifiers
- MONDO:0008195 OMIM:168300Orphanet:684
- Also known as
- Eulenburg disease · myotonia congenita intermittens · paramyotonia congenita · PMC · Von Eulenburg paramyotonia congenita
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