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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease dermatomyositis
Comorbidity C0085655|polymyositis
Sentences 3
PubMedID- 24587064 polymyositis (pm), together with dermatomyositis, belongs to idiopathic inflammatory myositis, which represents a heterogeneous group of autoimmune systemic diseases characterized by chronic muscle weakness and inflammatory cell infiltrates in skeletal muscle [7].
PubMedID- 24265670 To date, no cases were reported in which rapamycin was used to treat polymyositis, nevertheless, two cases of refractory dermatomyositis treated by rapamycin with good results have been published [33], [34], suggesting that the drug could have a beneficial effect in patient affected by autoimmune myositis.
PubMedID- 20392291 Distinct muscle expression of type 1 interferon-inducible genes in dermatomyositis (dm) compared with polymyositis (pm) and inclusion body myositis (ibm).

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