 Distal Myopathies
"Distal Myopathies" 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 genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive.
| Descriptor ID |
D049310
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| MeSH Number(s) |
C05.651.534.500.074 C10.668.491.175.500.074 C16.320.577.074
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| Concept/Terms |
Distal Myopathies- Distal Myopathies
- Myopathies, Distal
- Myopathy, Distal
- Distal Myopathy
- Muscular Dystrophy, Distal
- Distal Muscular Dystrophies
- Distal Muscular Dystrophy
- Muscular Dystrophies, Distal
Tibial Muscular Dystrophy- Tibial Muscular Dystrophy
- Muscular Dystrophies, Tibial
- Muscular Dystrophy, Tibial
- Udd Myopathy
- Myopathy, Udd
- Udd-Markesbery Muscular Dystrophy
- Muscular Dystrophy, Udd-Markesbery
- Udd Markesbery Muscular Dystrophy
- Finnish-Markesbery Muscular Dystrophy
- Finnish Markesbery Muscular Dystrophy
- Muscular Dystrophy, Finnish-Markesbery
- Udd Distal Myopathy
- Distal Myopathy, Udd
- Myopathy, Udd Distal
Welander Distal Myopathy- Welander Distal Myopathy
- Distal Myopathy, Welander
- Myopathy, Late Distal Hereditary
- Myopathy, Distal, Early-Onset, Autosomal Dominant
- Myopathy, Distal 1
- Distal 1 Myopathies
- Distal 1 Myopathy
- Myopathies, Distal 1
- Muscular Dystrophy, Distal, Late-Onset, Autosomal Dominant
- Distal Myopathy 1
- Distal Myopathy 1s
- Myopathy 1, Distal
- Myopathy 1s, Distal
- Laing Distal Myopathy
- Distal Myopathy, Laing
- Myopathy, Laing Distal
- Laing Early-Onset Distal Myopathy
- Laing Early Onset Distal Myopathy
- Myopathy, Distal, Swedish
Tibial Muscular Dystrophy, Tardive- Tibial Muscular Dystrophy, Tardive
- Distal Myopathy Markesbery-Griggs Type
- Distal Myopathy Markesbery Griggs Type
- Tardive Tibial Muscular Dystrophy
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Below are MeSH descriptors whose meaning is more general than "Distal Myopathies".
Below are MeSH descriptors whose meaning is more specific than "Distal Myopathies".
This graph shows the total number of publications written about "Distal Myopathies" by people in this website by year, and whether "Distal Myopathies" 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 |
|---|
| 2009 | 2 | 0 | 2 | | 2011 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Distal Myopathies" by people in Profiles.
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Feinstein-Linial M, Buvoli M, Buvoli A, Sadeh M, Dabby R, Straussberg R, Shelef I, Dayan D, Leinwand LA, Birk OS. Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture. BMC Med Genet. 2016 08 12; 17(1):57.
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Buvoli M, Buvoli A, Leinwand LA. Effects of pathogenic proline mutations on myosin assembly. J Mol Biol. 2012 Feb 03; 415(5):807-18.
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Armel TZ, Leinwand LA. Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes. J Mol Cell Cardiol. 2010 May; 48(5):1007-13.
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Senderek J, Garvey SM, Krieger M, Guergueltcheva V, Urtizberea A, Roos A, Elbracht M, Stendel C, Tournev I, Mihailova V, Feit H, Tramonte J, Hedera P, Crooks K, Bergmann C, Rudnik-Sch?neborn S, Zerres K, Lochm?ller H, Seboun E, Weis J, Beckmann JS, Hauser MA, Jackson CE. Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3. Am J Hum Genet. 2009 Apr; 84(4):511-8.
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