Central core disease, some forms of myotonia congenita, myotubular myopathy (possibly), some forms of nemaline myopathy, paramyotonia congenita and periodic paralysis follow the autosomal dominant pattern. One form of myotonia congenita and some forms of nemaline myopathy follow the autosomal recessive pattern. Some forms of myotubular myopathy follow the X-linked recessive pattern.