"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.
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.
- Alpha Sarcoglycanopathies
- Adhalinopathy, Primary
- Adhalinopathies, Primary
- Primary Adhalinopathies
- Primary Adhalinopathy
- Muscular Dystrophy Limb-Girdle with Alpha-Sarcoglycan Deficiency
- Muscular Dystrophy Limb Girdle with Alpha Sarcoglycan Deficiency
- Limb-Girdle Muscular Dystrophy, Type 2D
- Limb Girdle Muscular Dystrophy, Type 2D
- Alpha Sarcoglycanopathy
- Duchenne-Like Autosomal Recessive Muscular Dystrophy, Type 2
- Duchenne Like Autosomal Recessive Muscular Dystrophy, Type 2
- Muscular Dystrophy, Limb-Girdle, Type 2D
Below are MeSH descriptors whose meaning is more general than "Sarcoglycanopathies".
Below are MeSH descriptors whose meaning is more specific than "Sarcoglycanopathies".
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