Quadriceps myopathy (Q103464): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed an Item
‎Changed an Item
 
Property / Collection date
 
16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 16 August 2026 / rank
 
Normal rank

Latest revision as of 09:13, 17 August 2026

Quadriceps myopathy is a rare muscle disease predominately affecting the quadriceps muscles with clinical symptoms arising in adulthood. Etiologies can range from a form of limb-girdle muscular dystrophy to polymyositis. Genetic variants are suspected to arise from autosomal dominant, autosomal recessive, and X-linked recessive inheritance patterns, indicating that several gene products probably play a role in quadriceps myopathy pathology.
Language Label Description Also known as
default for all languages
ID_131281045
    English
    Quadriceps myopathy
    Quadriceps myopathy is a rare muscle disease predominately affecting the quadriceps muscles with clinical symptoms arising in adulthood. Etiologies can range from a form of limb-girdle muscular dystrophy to polymyositis. Genetic variants are suspected to arise from autosomal dominant, autosomal recessive, and X-linked recessive inheritance patterns, indicating that several gene products probably play a role in quadriceps myopathy pathology.

      Statements

      CID11:ID_131281045
      0 references
      dki-india-ID_131281045
      0 references
      Concluído
      0 references
      16 August 2026
      0 references