Table 2: Myopathies Associated with Dilative Cardiomyopathy and Stroke

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

CMD: congenital muscular dystrophy