Perifascicular muscle fiber atrophy

MedGen UID:: 488843
•Concept ID:: C0333757
•: Cell or Molecular Dysfunction; Disease or Syndrome

Synonyms:	Muscle fiber perifascicular atrophy; Perifascicular muscle fibre atrophy
SNOMED CT:	Muscle fiber perifascicular atrophy (87196003)

HPO:	HP:0100296

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVPerifascicular muscle fiber atrophy

Phenotypic abnormality
- Abnormality of the musculoskeletal system
  - Abnormality of the musculature
    - Abnormal skeletal muscle morphology
      - Abnormal muscle fiber morphology
        Perifascicular muscle fiber atrophy

Professional guidelines

PubMed

Idiopathic inflammatory myopathies in adults: A comparative study of Bohan and Peter and European Neuromuscular Center 2004 criteria.

Challa S, Jakati S, Uppin MS, Kannan MA, Liza R, Murthy Jagarlapudi MK
Neurol India 2018 May-Jun;66(3):767-771. doi: 10.4103/0028-3886.232296. PMID: 29766941

Anti-aminoacyl-tRNA synthetase-related myositis and dermatomyositis: clues for differential diagnosis on muscle biopsy.

Cerbelli B, Pisano A, Colafrancesco S, Pignataro MG, Biffoni M, Berni S, De Luca A, Riccieri V, Priori R, Valesini G, d'Amati G, Giordano C
Virchows Arch 2018 Mar;472(3):477-487. Epub 2017 Nov 16 doi: 10.1007/s00428-017-2269-x. PMID: 29147923

Anomalies in perifascicular muscle fibers as an differential-diagnostic criterion. I. Perifascicular atrophy in inflammatory myopathies.

Peiffer J, Bähr M
Clin Neuropathol 1987 May-Jun;6(3):123-32. PMID: 3608289

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Perifascicular muscle fiber atrophy

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