-
Calpainopathy is the most
common type of
autosomal recessive limb-girdle
muscular dystrophy (LGMD). It
preferentially affects the
muscles of the hip girdle...
- - Many
inherited myopathies may have
secondary myositis,
including calpainopathy, dysferlinopathy,
facioscapulohumeral muscular dystrophy, dystrophinopathy...
- LGMD1I 618129 CAPN3 LGMD R1 Also
referred to as "autosomal
dominant calpainopathy." LGMD D5
collagen 6-related
Bethlem myopathy 1 158810 COL6A1, COL6A2...
-
Distal Emery-Dreifuss
Facioscapulohumeral Limb–girdle
muscular dystrophy Calpainopathy Myotonic Oculopharyngeal National/International
Organizations Muscular...
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dystrophy (especially
calpainopathy),
scapuloperoneal myopathy,
mitochondrial myopathy,
Pompe disease, and polymyositis.
Calpainopathy and scapuloperoneal...
- calpain3-related LGMD D5
collagen 6-related LGMD R1 calpain3-related (
Calpainopathy) LGMD R2 dysferlin-related LGMD R3 α-sarcoglycan-related LGMD R4 β-sarcoglycan-related...
- Calderon–Gonzalez–Cantu
syndrome Calloso genital dysplasia Callus disease Calpainopathy Calvarial doughnut lesions-bone
fragility syndrome Calvarial hyperostosis...
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Piluso G,
Feingold J (2004). "Prevalence of the 550delA
mutation in
calpainopathy (LGMD 2A) in Croatia". Am. J. Med. Genet. A. 125A (2): 152–6. doi:10...
