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
Experts
1. | Aguilar Castillo, Sergio De Jesús:
1 article
(04/2022)
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2. | Camargo Coronel, Adolfo:
1 article
(04/2022)
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3. | Hernández Vázquez, José Ramiro:
1 article
(04/2022)
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4. | Hernández Zavala, Mario Raúl:
1 article
(04/2022)
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5. | Jiménez Balderas, Francisco Javier:
1 article
(04/2022)
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6. | Mandinabeitia Rodríguez, Pedro:
1 article
(04/2022)
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7. | Quiñones Moya, Horacio:
1 article
(04/2022)
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8. | Zamora Zarco, Sandy:
1 article
(04/2022)
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9. | Herings, Ron M C:
1 article
(12/2002)
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10. | Klungel, Olaf H:
1 article
(12/2002)
|
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to familial Idiopathic inflammatory myopathy: