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central core disease

Medical Definition

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)
Related Codes (1)
Code
Description
Billable
Details
G71.29Other congenital myopathy

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