Muscular Dystrophies, Limb-Girdle
"Muscular Dystrophies, Limb-Girdle" 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 heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).
| Descriptor ID |
D049288
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| MeSH Number(s) |
C05.651.534.500.280 C10.668.491.175.500.149 C16.320.577.280
|
| Concept/Terms |
Muscular Dystrophies, Limb-Girdle- Muscular Dystrophies, Limb-Girdle
- Muscular Dystrophies, Limb Girdle
- Myopathic Limb-Girdle Syndrome
- Muscular Dystrophy, Limb-Girdle
- Muscular Dystrophy, Limb Girdle
- Limb-Girdle Syndrome
- Limb-Girdle Muscular Dystrophies
- Limb Girdle Muscular Dystrophies
- Limb-Girdle Muscular Dystrophy
- Limb Girdle Muscular Dystrophy
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Below are MeSH descriptors whose meaning is more general than "Muscular Dystrophies, Limb-Girdle".
Below are MeSH descriptors whose meaning is more specific than "Muscular Dystrophies, Limb-Girdle".
This graph shows the total number of publications written about "Muscular Dystrophies, Limb-Girdle" by people in this website by year, and whether "Muscular Dystrophies, Limb-Girdle" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Muscular Dystrophies, Limb-Girdle" by people in Profiles.
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Expression, purification, and structural analysis of the full-length human integral membrane protein ?-sarcoglycan. Protein Expr Purif. 2020 03; 167:105525.
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Myotilin overexpression enhances myopathology in the LGMD1A mouse model. Muscle Nerve. 2008 May; 37(5):663-7.
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Transgenic mice expressing the myotilin T57I mutation unite the pathology associated with LGMD1A and MFM. Hum Mol Genet. 2006 Aug 01; 15(15):2348-62.