Distal myopathy, Miyoshi type (Q101273): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
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. | |||
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 |
||
| 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. |
