How is susceptibility to MH inherited?
Susceptibility to MH is thought to be inherited
by auto-somal dominant pattern with mixed penetrance, although an autosomal
recessive form exists as well. Multiple muta-tions for the ryanodine receptor
of the sarcoplasmic retic-ulum are causative. Other genes may be involved as
well. The identification of a single causative gene, therefore, is not
possible. Siblings and children of MH-susceptible individuals experience a 50%
risk of susceptibility.
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