Necrotic myopathy (Q103465): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/124501922 / rank | |||
Normal rank | |||
Revision as of 09:13, 17 August 2026
Group of myopathic disorders characterized by the predominant pathological feature of necrosis of muscle fibers in the absence of substantial lymphocytic inflammatory infiltrates. Most commonly divided into immune-mediated (IMNM) and non-immune mediated (NIMNM). Both IMNM and NIMNM are typically characterized by proximal weakness, although the severity can vary.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_124501922 |
||
| English | Necrotic myopathy |
Group of myopathic disorders characterized by the predominant pathological feature of necrosis of muscle fibers in the absence of substantial lymphocytic inflammatory infiltrates. Most commonly divided into immune-mediated (IMNM) and non-immune mediated (NIMNM). Both IMNM and NIMNM are typically characterized by proximal weakness, although the severity can vary. |
