Structured Summary
Abstract
Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
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Classification
Broader headings
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MeSH Record
Synonyms
8 entry terms
- Myositis, Inclusion Body
- Inclusion Body Myositides
- Myositides, Inclusion Body
- Inclusion Body Myopathy, Sporadic
- Inclusion Body Myositis, Sporadic
- Myopathy, Inclusion Body, Sporadic
- Myositis, Inclusion Body, Sporadic
- Sporadic Inclusion Body Myositis
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
Indexing Annotation
do not coord with INCLUSION BODIES but coord with INCLUSION BODIES, VIRAL if relevant (IM or NIM)
MeSH Record
History Note
96
MeSH Record
Previous Indexing
- Myositis (1968-1995)
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Tree Numbers
AMA Style
References
- National Library of Medicine. Inclusion Body Myositis. Medical Subject Headings (MeSH). 2026. Unique ID D018979. http://id.nlm.nih.gov/mesh/2026/D018979
- Inclusion Body Myositis. In: Wikipedia. https://en.wikipedia.org/wiki/Inclusion_body_myositis
- Inclusion Body Myositis. In: Wikidata. https://www.wikidata.org/wiki/Q1848471