Structured Summary
Abstract
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)
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
9 entry terms
- Central Core Disease
- Central Core Disease of Muscle
- Myopathy, Central Core
- Shy-Magee Syndrome
- Central Core Diseases
- Central Core Myopathies
- Myopathies, Central Core
- Shy Magee Syndrome
- Syndrome, Shy-Magee
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2000; for CENTRAL CORE DISEASE & SHY-MAGEE SYNDROME use NEMALINE MYOPATHY 1994-1999
MeSH Record
Previous Indexing
- Muscles/enzymology (1963-1999)
- Muscular Atrophy (1963-1999)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Central Core Myopathy. Medical Subject Headings (MeSH). 2026. Unique ID D020512. http://id.nlm.nih.gov/mesh/2026/D020512
- Central Core Myopathy. In: Wikipedia. https://en.wikipedia.org/wiki/Central_core_disease
- Central Core Myopathy. In: Wikidata. https://www.wikidata.org/wiki/Q638975