Common

Myotonia congenita

Genetic disorder causing muscles to delay relaxing after contraction

Myotonia congenita

Common card · No. 420935

Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder. The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles (myotonia) and rigidity. Symptoms include delayed relaxation of the muscles after voluntary contraction (myotonia), and may also include stiffness, hypertrophy (enlargement), transient weakness in some forms of the disorder (from certain genetic mutations), severe masseter spasm, and cramping. The condition is sometimes referred to as fainting goat syndrome, as it is responsible for the eponymous 'fainting' seen in fainting goats when presented with a sudden stimulus. Of note, myotonia congenita is associated with increased risk of malignant hyperthermia (MH) during general anaesthetic.

Read on Wikipedia · Image Jules Dejerine, Augusta Klumpke-Dejerine, Licence Ouverte

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