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Chapter 6 - Diseases of the nervous system (G00-G99)»Diseases of myoneural junction and muscle (G70-G73)»Myotonia congenita (G71.12)

G71.12

Myotonia congenita

Related indications (MeSH) (1)

Myotonia Congenita4 drugs (4 approved)

Inherited myotonic disorders with early childhood onset MYOTONIA. Muscular hypertrophy is common and myotonia may impair ambulation and other movements. It is classified as Thomsen (autosomal dominant) or Becker (autosomal recessive) generalized myotonia mainly based on the inheritance pattern. Becker type is also clinically more severe. An autosomal dominant variant with milder symptoms and later onset is known as myotonia levior. Mutations in the voltage-dependent skeletal muscle chloride channel are associated with the disorders.