Myopathy | Reference | Stroke |
---|---|---|
Muscular dystrophies | ||
Dystrophinopathies | [16,102] | [10,16,17] |
Limb girdle muscular dystrophies | [103,104] | NR |
Laminopathies | [81,105-107] | NR |
LGMD1B | [108] | NR |
LGMD1E | [108] | NR |
LGMD2D-F | [108] | NR |
LGMD2I | [108,109] | NR |
Congential muscular dystrophies | ||
Fukuyama type CMD | [110] | NR |
Merosin-deficient CMD | [111] | NR |
Myofibrillar myopathies | [112] | NR |
Desminopathy | [113] | NR |
Other | ||
Vacuolar myopathy (LAMP2) | [114,115] | NR |
Barth syndrome | [116,117] | [18] |
McLeod syndrome | [118] | NR |
Reducing body myopathy | [119,120] | NR |
Congenital myopathies | ||
Nemaline myopathy | [121, 122] | NR |
Central core disease | [123] | NR |
Centronuclear myopathy | [124,125] | NR |
Congenital fiber type dysproportion | [96,126,127] | NR |
Metabolic myopathies | ||
Glycogenosis type IV | [128] | NR |
Primary carnitin deficiency | [129] | NR |
Mitochondrial disorders | [130,131] | NR |
Kearns-Sayre syndrome | [132] | NR |