eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | myositis |
| Symptom | C0004093|weakness |
| Sentences | 7 |
| PubMedID- 21457520 | The idiopathic inflammatory myopathies (iims) poly-myositis (pm) and dermatomyositis (dm) are heterogeneous conditions that are historically diagnosed by proximal muscle weakness, evidence of muscle inflammation or necrosis, and characteristic skin lesions . |
| PubMedID- 25798107 | However, among the 27 differentially methylated genes several hox genes (hoxc11, hoxd3 and hoxd4) and the developmental transcription factor wt1 were found hypomethylated in juvenile dm samples, as well as in other types of idiopathic inflammatory myopathies (iims) with muscle weakness, such as juvenile polymyositis (wang et al., 2012). |
| PubMedID- 22955479 | Dermatomyositis is a rare autoimmune inflammatory myopathy with proximal muscle weakness and skin affection. |
| PubMedID- 19906360 | Known as idiopathic inflammatory myopathies (iim), they all share the presence of considerable weakness due to muscle inflammation and necrosis. |
| PubMedID- 24648807 | Dermatomyositis (dm) is an idiopathic inflammatory myopathy with progressive, symmetrical weakness of the proximal muscles and characteristic cutaneous manifestations such as poikiloderma 1. |
| PubMedID- 21470434 | Moreover, when inflammatory myopathies present with a significant weakness at diagnosis, they carry an unfavorable impact on prognosis. |
| PubMedID- 26417430 | Inflammatory myopathies are a group of diseases that involve chronic muscle inflammation (myositis) accompanied with muscle weakness . |
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