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Interdisciplinary CompetenceMolecular Diagnostics
Know how in the analysis of genetic material.
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IllnessMyotonia congenita

Summary

Short information

Curated single gene sequence analysis according to the clinical suspicion Myotonia congenita

ID
MS7030
Number of genes
1 Accredited laboratory test
Examined sequence length
3,0 kb (Core-/Base-Genes)
- (Extended panel)
Analysis Duration
on request
Material
  • EDTA-anticoagulated blood (3-5 ml)
Diagnostic indications

NGS +

 

Gene panel

Selected genes

NameExon Length (bp)OMIM-GHeredity
CLCN12967AD and/or AR

Informations about the disease

Clinical Comment

Myotonia congenita affects skeletal muscles beginning in childhood with bouts of sustained myotonia of any muscles, including of the face and tongue, but most often in the legs causing stiffness sometimes with warm-up effect. The two major types are designated Thomsen disease and Becker disease as distinguished by the severity of symptoms and patterns of inheritance. Becker disease usually appears later in childhood causing more severe stiffness. Becker disease patients often experience temporary attacks of muscle weakness, sometimes permanent over time. Mutations in the CLCN1 gene alter structure and/or function of chloride channels. Thomsen disease is transmitted in an autosomal dominant pattern, Becker disease is inherited in an autosomal recessive manner. The phenotypic manifestations of the pathogenic variants in CLCN1 can be variable even within the same family; many autosomal dominant pathogenic variants can be associated with reduced penetrance. Both, the analytical sensitivity and specificity are close to 100%, the clinical sensitivity and specificity are dependent on variable factors such as age and/or family history.

 

Synonyms
  • Alias: Non-dystrophic skeletal muscle disorder
  • Alias: Thomsen disease + Becker disease
  • Myotonia congenita, AD (CLCN1)
  • Myotonia congenita, AR (CLCN1)
  • Myotonia levior, AR (CLCN1)
Heredity, heredity patterns etc.
  • AD and/or AR
OMIM-Ps
ICD10 Code
G71.1

Bioinformatics and clinical interpretation

No text defined