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Myotonia congenita
Definition:
Myotonia congenita is an inheritable congenital (present from birth) disorder characterized by slow relaxation of voluntary muscles, such as those in the legs. Alternative Names:
Thomsen's disease
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Causes, incidence, and risk factors:
Myotonia congenita can be either an autosomal dominant or autosomal recessive disease. With the autosomal dominant form, a person only needs to inherit the mutation from one parent to be affected. Inheriting the recessive form means a person must inherit the mutation from both parents to be affected. The gene that causes this condition resides on chromosome 7. The cause of myotonia congenita is believed to be an abnormality in the chloride channels of muscle cells (chloride ions are required for a muscle to relax). The abnormal chloride channels also cause an accumulation of potassium outside the cells and an activation of sodium channels in the muscle cells (sodium ions trigger muscle contraction). When the cells have more than enough sodium but not enough chloride, abnormal repetitive electrical discharges cause a stiffness called myotonia.
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