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familial Idiopathic inflammatory myopathy

Variable symptoms usually include progressive muscle weakness. May present similarly to juvenile dermatomyositis, but progress to systemic involvement with death by 4 years of age. There may also be no systemic invlovement in adults , with progression similar to POLYMYOSITIS. OMIM: 160750
Also Known As:
Idiopathic inflammatory myopathy, familial; Idiopathic myopathy; Myopathy, familial idiopathic inflammatory
Networked: 4 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Myocarditis (Carditis)
2. Macular Edema
3. COVID-19

Experts

1. Aguilar Castillo, Sergio De Jesús: 1 article (04/2022)
2. Camargo Coronel, Adolfo: 1 article (04/2022)
3. Hernández Vázquez, José Ramiro: 1 article (04/2022)
4. Hernández Zavala, Mario Raúl: 1 article (04/2022)
5. Jiménez Balderas, Francisco Javier: 1 article (04/2022)
6. Mandinabeitia Rodríguez, Pedro: 1 article (04/2022)
7. Quiñones Moya, Horacio: 1 article (04/2022)
8. Zamora Zarco, Sandy: 1 article (04/2022)
9. Herings, Ron M C: 1 article (12/2002)
10. Klungel, Olaf H: 1 article (12/2002)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to familial Idiopathic inflammatory myopathy:
1. Fibric Acids (Fibrates)IBA
2. Hydroxymethylglutaryl-CoA Reductase Inhibitors (HMG-CoA Reductase Inhibitors)IBA
3. VaccinesIBA
4. Messenger RNA (mRNA)IBA
5. Retinaldehyde (Retinal)IBA
6. Oxidoreductases (Dehydrogenase)IBA
7. LipidsIBA
8. Coenzyme A (CoA)IBA