Distal myopathy, Miyoshi type (Q101273): Difference between revisions
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CID11:ID_1844018161 | |||||||||||||||
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dki-india-ID_1844018161 | |||||||||||||||
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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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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 |
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| 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. |
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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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