Hypomyopathic juvenile dermatomyositis (Q92500): Difference between revisions
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Dermatomiosite juvenil hipomiopática é um subgrupo de dermatomiosite de início na infância caracterizado pela ausência de sintomas subjetivos, mas com evidência subclínica de inflamação muscular na biópsia muscular, na eletromiografia ou em outros procedimentos. | |||
| description / en | description / en | ||
Hypomyopathic juvenile dermatomyositis is young-onset subset of dermatomyositis characterised by a lack of subjective symptoms but with subclinical evidence of muscle inflammation on muscle biopsy, electromyography, or other procedures. | |||
Revision as of 07:38, 16 August 2026
Hypomyopathic juvenile dermatomyositis is young-onset subset of dermatomyositis characterised by a lack of subjective symptoms but with subclinical evidence of muscle inflammation on muscle biopsy, electromyography, or other procedures.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2020758398 |
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| English | Hypomyopathic juvenile dermatomyositis |
Hypomyopathic juvenile dermatomyositis is young-onset subset of dermatomyositis characterised by a lack of subjective symptoms but with subclinical evidence of muscle inflammation on muscle biopsy, electromyography, or other procedures. |
