Mesh term Myopathy, Central Core
Browse to parent terms:Myopathies, Structural, Congenital
Description
An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a condensation of myofibrils and myofibrillar material in the central portion of each muscle fiber. (Adams et al., Principles of Neurology, 6th ed, p1452)Search for this term in our Faculty Database
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