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World J Cardiol. Apr 26, 2012; 4(4): 103-111
Published online Apr 26, 2012. doi: 10.4330/wjc.v4.i4.103
Published online Apr 26, 2012. doi: 10.4330/wjc.v4.i4.103
HCM | DCM | ARVC | RCM | Unclassified | |
Familial | Familial, unknown gene | Familial, unknown gene | Familial, unknown gene | Familial, unknown gene | Familial, unknown gene |
Sarcomeric protein mutations | Sarcomeric protein mutations (see HCM) | Intercalated disc protein mutations | Sarcomeric protein mutations | Left ventricular Non-compaction | |
β myosin heavy chain | Z-band | Plakoglobin | Troponin I (RCM +/- HCM) | Barth syndrome | |
Cardiac myosin binding protein C | Muscle LIM protein | Desmoplakin | Essential light chain of myosin | Lamin A/C | |
Cardiac troponin 1 | TCAP | Plakophilin 2 | Familial amyloidosis | ZASP | |
Troponin T | Cytoskeletal genes | Desmoglein 2 | Transthyretin (RCM + neuropathy) | α-dystrophin | |
α-tropomyosin | Dystrophin | Desmocollin 2 | Apolipoprotein (RCM + neuropathy) | ||
Essential myosin light chain | Desmin | Cardiac RyR2 | Desminopathy | ||
Regulatory myosin light chain | Metavinculin | TGFβ3 | Pseuxanthoma elasticum | ||
Cardiac actin | Sarcoglycan complex | Haemochromatosis | |||
α-myosin heavy chain | CRYAB | Anderson-Fabry disease | |||
Titin | Epicardin | Glycogen storage disease | |||
Troponin C | Nuclear membrane | ||||
Muscle LIM protein | Lamin A/C | ||||
Glycogen storage disease (e.g., Pompe; PRKAG2, Forbes’, Danon) | Emerin | ||||
Lysosomal storage disease (e.g., Anderson-Fabry, Hurler’s) | Mildly dilated cardiomyopahy | ||||
Disorders of fatty metabolism | Intercalated disc protein mutations (see ARVC) | ||||
Carnitine deficiency | Mitochondrial myopathy | ||||
Phosphorylase B kinase deficiencz | Dystrophies | ||||
Mitochondrial cytopathies | |||||
Syndromic HCM | |||||
Noonan syndrome | |||||
LEOPARD syndrome | |||||
Friedriech’s ataxia | |||||
Beckwith-Wiedermann syndrome | |||||
Swyer’s syndrome | |||||
Other | |||||
Phospholamban promotor | |||||
Familal amyloid | |||||
Non familial | Obesity | Myocarditis (infective/toxic/autoimmune) | Inflammation? | Amyloid (AL/prealbumin) | Tako Tsubo cardiomyopathy |
Infants of diabetic mothers | Kawasaki disease | Scleroderma | |||
Athletic training | Eosinophilic (Churg Strauss syndrome) | Endomyocardial fibrosis | |||
Amyloid (AL/prealbumin) | Viral persistence | Hypereosinophilic syndrome | |||
Drugs | Idiopathic | ||||
Pregnancy | Chromosomal cause | ||||
Endocrine | Drugs (serotonin, methysergide, ergotamine) | ||||
Nutritional - thiamine, carnitine, selenium, hypophosphatemia, hypocalcemia | |||||
Alcohol | Carcinoid heart disease | ||||
Tachycardiomyopathy | Metastatic cancers | ||||
Radiation | |||||
Drugs (anthracyclines) |
- Citation: McDermott S, O’Neill AC, Ridge CA, Dodd JD. Investigation of cardiomyopathy using cardiac magnetic resonance imaging part 1: Common phenotypes. World J Cardiol 2012; 4(4): 103-111
- URL: https://www.wjgnet.com/1949-8462/full/v4/i4/103.htm
- DOI: https://dx.doi.org/10.4330/wjc.v4.i4.103