Neuromuscular HOMEepAGE
neuromuscular.wustl.edu
/
A–Z

Inflammatory & Immune Myopathies (IIM): Acquired

MitochondrialImmune/Antibody
W
View full entry on WUSTL Neuromuscular
antibody/infmyop.htm#Inflammatory & Immune Myopathies (IIM): Acquired

Overview

From WUSTL Neuromuscular

IIM: General Features Signs & Lab findings Aldolase Antibodies Calcinosis CK: Serum Electrodiagnostic HLA & Genotypes Neoplasm associations Other systemic Pain Prognosis Skin lesions Syndromes Treatment Weakness Pathology Differential disagnosis Pathology Animal Models Experimental autoimmune myositis MHC class I upregulation History Dermatomyopathies IIM: Possible 1st case, Hepp 1887 Berliner Klinische Wochenschrift Immune or Inflammatory Myopathies (IIM): Syndromes Immune myopathies General aspects Clinical Laboratory Subtypes & Comparative features Brachio-Cervical Inflammatory (BCIM) Check

Related Conditions

Shared genes
ANTIBODIES IN CONNECTIVE TISSUE DISORDERS
ASSOCIATEDANTIBODIESPL-12
Asymmetric Myopathic Weakness
VAMP
DERMATOLOGIC DISORDERS & NEUROMUSCULAR DISEASE
VP
DERMATOMYOPATHIES, IMMUNE
VP
Finger Flexion Weakness
VAMP
Granulomatous Myopathies
VAMP
Immune & Inflammatory Myopathies: Neoplasm Associations
VPVAMP
Inclusion Body Myositis (IBM)
VAMPIADRB1

External Resources

WUSTL Neuromuscular
Washington University Disease Center
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.