 Myopathies, Structural, Congenital
"Myopathies, Structural, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A heterogeneous group of diseases characterized by the early onset of hypotonia, developmental delay of motor skills, non-progressive weakness. Each of these disorders is associated with a specific histologic muscle fiber abnormality.
| Descriptor ID |
D020914
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| MeSH Number(s) |
C05.651.575 C10.668.491.550
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| Concept/Terms |
Myopathies, Structural, Congenital- Myopathies, Structural, Congenital
- Structural Myopathies, Congenital
- Non-Progressive Myopathies, Congenital
- Non Progressive Myopathies, Congenital
- Congenital Non-Progressive Myopathies
- Congenital Non Progressive Myopathies
- Congenital Non-Progressive Myopathy
- Myopathies, Congenital Non-Progressive
- Myopathy, Congenital Non-Progressive
- Non-Progressive Myopathy, Congenital
- Congenital Structural Myopathies
- Congenital Structural Myopathy
- Myopathies, Congenital Structural
- Myopathy, Congenital Structural
- Structural Myopathy, Congenital
Tubular Aggregate Myopathy- Tubular Aggregate Myopathy
- Aggregate Myopathies, Tubular
- Aggregate Myopathy, Tubular
- Myopathies, Tubular Aggregate
- Tubular Aggregate Myopathies
- Myopathy, Tubular Aggregate
Centronuclear Myopathy- Centronuclear Myopathy
- Centronuclear Myopathies
- Myopathies, Centronuclear
- Myopathy, Centronuclear
- Myotubular Myopathy 1
- Myopathy, Myotubular
- Myopathies, Myotubular
- Myotubular Myopathies
Congenital Fiber Type Disproportion- Congenital Fiber Type Disproportion
- Myopathy, Congenital, With Fiber-Type Disproportion
- Fiber-Type Disproportion Myopathy, Congenital
- Fiber Type Disproportion Myopathy, Congenital
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Below are MeSH descriptors whose meaning is more general than "Myopathies, Structural, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Myopathies, Structural, Congenital".
This graph shows the total number of publications written about "Myopathies, Structural, Congenital" by people in UAMS Profiles by year, and whether "Myopathies, Structural, Congenital" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 | | 2015 | 2 | 0 | 2 | | 2014 | 1 | 0 | 1 | | 2008 | 2 | 0 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Myopathies, Structural, Congenital" by people in Profiles over the past ten years.
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Malatesta L, Arya K, Gokden M, Stefans V, Veerapandiyan A. BAG3 Myopathy Presenting With Prominent Neuropathic Phenotype and No Cardiac or Respiratory Involvement: A Case Report and Literature Review. J Clin Neuromuscul Dis. 2020 Jun; 21(4):230-239.
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Vincent AE, Grady JP, Rocha MC, Alston CL, Rygiel KA, Barresi R, Taylor RW, Turnbull DM. Mitochondrial dysfunction in myofibrillar myopathy. Neuromuscul Disord. 2016 10; 26(10):691-701.
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Smith BK, Renno MS, Green MM, Sexton TM, Lawson LA, Martin AD, Corti M, Byrne BJ. Respiratory motor function in individuals with centronuclear myopathies. Muscle Nerve. 2016 02; 53(2):214-21.
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Smith BK, Renno MS, Martin AD, Corti M, Byrne BJ. Reply: Respiratory motor function in centronuclear myopathy. Muscle Nerve. 2016 04; 53(4):660-1.
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