Distal myopathy, Miyoshi type (Q101273): 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/1844018161 / rank
 
Normal rank

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.

      Statements