Distal myopathy, Miyoshi type (Q101273): Difference between revisions
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A miopatia de Miyoshi (disferlinopatia) pertence ao grupo heterogêneo de miopatias distais e é clinicamente caracterizada por fraqueza e atrofia das panturrilhas, que às vezes é assimétrica, levando à incapacidade de pular, correr ou andar na ponta dos pés, e que subsequentemente progride para a parte superior e membros inferiores. Os músculos faciais, bulbares e cardíacos são poupados. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Miyoshi myopathy (dysferlinopathy) belongs to the heterogeneous group of distal myopathies, and is clinically characterised by weakness and atrophy of the calves, which is sometimes asymmetrical, leading to inability to jump, run or walk on tiptoes, and that subsequently progresses to the upper and lower limbs. Facial, bulbar and cardiac muscles are spared. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1844018161 / rank | |||||||||||||||
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CID11:ID_1844018161 | |||||||||||||||
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dki-india-ID_1844018161 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1844018161 / rank | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 18:04, 16 August 2026
Miyoshi myopathy (dysferlinopathy) belongs to the heterogeneous group of distal myopathies, and is clinically characterised by weakness and atrophy of the calves, which is sometimes asymmetrical, leading to inability to jump, run or walk on tiptoes, and that subsequently progresses to the upper and lower limbs. Facial, bulbar and cardiac muscles are spared.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1844018161 |
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| English | Distal myopathy, Miyoshi type |
Miyoshi myopathy (dysferlinopathy) belongs to the heterogeneous group of distal myopathies, and is clinically characterised by weakness and atrophy of the calves, which is sometimes asymmetrical, leading to inability to jump, run or walk on tiptoes, and that subsequently progresses to the upper and lower limbs. Facial, bulbar and cardiac muscles are spared. |
Statements
CID11:ID_1844018161
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dki-india-ID_1844018161
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Concluído
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15 August 2026
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