Inclusion body myositis (IBM) is the most common inflammatory muscle disease in older adults, combining autoimmune inflammation with muscle degeneration and causing progressive weakness in both proximal muscles near the torso and distal muscles near the hands and feet. It typically begins after age 45, with mean onset between 61 and 68, and affects men more often than women, at roughly 46 per million people. Early signs include frequent tripping, difficulty climbing stairs and foot drop, followed by trouble manipulating the fingers and weakness of the finger flexors and ankle dorsiflexors; difficulty swallowing affects 40 to 85 percent of cases and can cause serious complications. IBM does not significantly shorten life expectancy, but most patients need a walker or wheelchair within five to ten years of onset, and as of 2019 there was no effective treatment.
Facts
Classification
ICD-10 ChapterVI: Diseases of the Nervous System 2 Communicable or Non-communicable Transmission Route Prevalence Band Sources
1. Inclusion body myositis (Wikipedia)
lead sentence 1
Inclusion body myositis (IBM) () (sometimes called sporadic inclusion body myositis, sIBM) is the most common inflammatory muscle disease in older adults.
Lead
Inclusion body myositis (IBM) () (sometimes called sporadic inclusion body myositis, sIBM) is the most common inflammatory muscle disease in older adults.
View the Source2. Monarch Initiative: inclusion body myositis - Monarch Initiative MONDO:0007827
Monarch InitiativeCross reference: ICD10CMQuote, Cross reference: ICD10CM
ICD10CM:G72.41
View the Source 3. Orphadata (Orphanet): Orphadata epidemiology, ORPHAcode 611
Orphadata (Orphanet)Orphanet epidemiology, ORPHAcode 611Quote, Orphanet epidemiology, ORPHAcode 611
"PrevalenceClass": "1-9 / 1 000 000", "PrevalenceGeographic": "Europe", "PrevalenceQualification": "Value and class", "PrevalenceType": "Point prevalence"
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