eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | inclusion body myositis |
| Symptom | C0004093|weakness |
| Sentences | 3 |
| PubMedID- 24365315 | Idiopathic inflammatory myopathies (iims), except for sporadic inclusion body myositis (sibm), present with subacute symmetrical weakness of the limb girdle muscles, an elevated serum creatine kinase activity, and inflammatory cells in the muscle biopsy (necrotizing autoimmune myopathy being an exception). |
| PubMedID- 20127578 | Patterns of weakness in inclusion body myositis and facioscapulohumeral muscular dystrophy are illustrated. |
| PubMedID- 23342768 | An inflammatory myopathy, inclusion body myositis (ibm) presents with progressive muscle weakness against a background of elevated creatine kinase and diffuse endomysial damage. |
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