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Inclusion Body Myositis (IBM)

MitochondrialAutosomal DominantImmune/AntibodyOMIM 607182
W
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antibody/infmyop.htm#Inclusion Body Myositis (IBM) 22

Overview

From WUSTL Neuromuscular

Nosology: Pathology groups Inflammatory Myopathy with Vacuoles, Aggregates & Mitochondrial Pathology (IM-VAMP) Inflammatory myopathy + Mitochondrial pathology Epidemiology 94 Sporadic: No family history Males Preponderance: 57% to 75% Later onset Frequency (Prevalence) General populations: 1 to 10/106 > 50 years of age: 139/106 Norway: 33/106 Turkey: 1/106 HIV 103 IM-VAMP is most common associated inflammatory myopathy May present with Onset age: 10 years younger than other IBM Proximal weakness Serum CK high NT5C1A antibodies (64%) HTLV Sarcoid & Granulomatous myopathies May have association

OMIM Entries

OMIM #607182OMIM #610525

Related Conditions

Shared genes
Asymmetric Myopathic Weakness
VAMP
CMT IA
PMP-22GENETM
Finger Flexion Weakness
VAMP
Granulomatous Myopathies
VAMP
Immune & Inflammatory Myopathies: Neoplasm Associations
VPVAMP
Inflammatory & Immune Myopathies (IIM): Acquired
RNAVAMPINCLUSION
Inflammatory Myopathy + Mitochondrial Pathology in muscle (IM-Mito), subtype of IM-VAMP
VAMP
Isaac's Syndrome
ACHRRIADRB1

External Resources

WUSTL Neuromuscular
Washington University Disease Center
OMIM
Online Mendelian Inheritance in Man
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.