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Myasthenia gravis , progressive muscular dystrophy , periodic paralysis more common. The remaining myopathy are rare.Autoimmune disease myasthenia gravis passed to the skeletal muscle neuromuscular junction dysfunction based. Showed the involvement of skeletal muscle fatigue easily and appears gravis.

Dermatomyositis, a rare connective tissue disease, mainly proximal limb muscle aches weakness and characteristic skin lesions.

Progressive muscular dystrophy patients with primary muscle degeneration to aggravate the symmetry gravis, muscular dystrophy is a genetic disease visual impact muscle building review

Myotonic diseases a group of rare genetic diseases. Typical manifestations of myotonia, ie voluntary movement began or tonic contraction of muscles stimulated soon need a few seconds to ten a few seconds to relaxation, resulting limbs were stiff, the action is not working, hand shaking hands with people not immediately released. 

Atrophic or dystrophic myotonia (Steiner's disease, muscle rigidity, muscle weakness and muscle atrophy more prominent), congenital myotonia (Thomson's disease onset in infancy with muscle hypertrophy), congenital Vice the myotonia s disease, childhood disease, manifested as myotonia and paroxysmal weakness, obvious the Myotonia to hemifacial). No special treatment. Quinine, procainamide, adrenocorticotropic hormone ease symptoms.

Congenital myopathy such as rod-shaped body myopathy, myopathy central axis empty disease, muscular tube performance (both muscle weakness, hypotonia, muscle fibers are rod-shaped body, the central axis null myotubes); congenital muscular fibers Type uneven; the multiple axes empty disease; fingerprint body myopathy.