Calpainopathy is the most common type of autosomal recessive limb-girdle muscular dystrophy (LGMD). It preferentially affects the muscles of the hip girdle...
11 KB (955 words) - 06:23, 17 September 2024
- Many inherited myopathies may have secondary myositis, including calpainopathy, dysferlinopathy, facioscapulohumeral muscular dystrophy, dystrophinopathy...
11 KB (1,020 words) - 05:31, 10 August 2024
LGMD1I 618129 CAPN3 LGMD R1 Also referred to as "autosomal dominant calpainopathy." LGMD D5 collagen 6-related Bethlem myopathy 1 158810 COL6A1, COL6A2...
35 KB (2,770 words) - 01:46, 18 September 2024
Distal Emery-Dreifuss Facioscapulohumeral Limb–girdle muscular dystrophy Calpainopathy Myotonic Oculopharyngeal National/International Organizations Muscular...
114 KB (12,648 words) - 07:58, 15 September 2024
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...
9 KB (902 words) - 15:36, 8 September 2024
dystrophy (especially calpainopathy), scapuloperoneal myopathy, mitochondrial myopathy, Pompe disease, and polymyositis. Calpainopathy and scapuloperoneal...
175 KB (16,431 words) - 20:09, 29 September 2024
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...
11 KB (1,368 words) - 02:59, 30 July 2024
Calderon–Gonzalez–Cantu syndrome Calloso genital dysplasia Callus disease Calpainopathy Calvarial doughnut lesions-bone fragility syndrome Calvarial hyperostosis...
40 KB (3,657 words) - 03:02, 17 August 2024