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Thomsen and Becker disease

MONDO:0009710

A rare, genetic, skeletal muscle channelopathy characterized by slow muscle relaxation after contraction (myotonia).

Also known as: myotonia congenita, Batten-Turner congenital myopathy, myopathy, congenital

9 clinical trials for this condition and its sub-types.

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Sub-types

Myotonia congenita, autosomal dominant (0) Myotonia congenita, autosomal recessive (0)

Broader categories

Disease (618) Nervous system disorder (217) Neuromuscular disease (98) Human disease (14) Disease by molecular mechanism (2) Disease by body system or component (0) Disease by developmental or physiological process (0) Muscular channelopathy (0)
Trials to join now! 5 Not yet recruiting 1 Completed 3
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