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Sarcoglycanopathies

"Sarcoglycanopathies" 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.

expand / collapse MeSH information
Deficiencies or mutations in the genes for the SARCOGLYCAN COMPLEX subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.


expand / collapse Publications
This graph shows the total number of publications written about "Sarcoglycanopathies" by people in this website by year, and whether "Sarcoglycanopathies" was a major or minor topic of these publications.
Below are the most recent publications written about "Sarcoglycanopathies" by people in Profiles.
  1. Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD study. BMC Neurol. 2024 Mar 15; 24(1):96.
    View in: PubMed
  2. Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D. Skelet Muscle. 2021 01 07; 11(1):2.
    View in: PubMed
  3. Nanospan, an alternatively spliced isoform of sarcospan, localizes to the sarcoplasmic reticulum in skeletal muscle and is absent in limb girdle muscular dystrophy 2F. Skelet Muscle. 2017 06 06; 7(1):11.
    View in: PubMed
  4. Sarcoid polyneuropathy masquerading as chronic inflammatory demyelinating polyneuropathy. Muscle Nerve. 2015 Oct; 52(4):664-8.
    View in: PubMed