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©2012 Baishideng Publishing Group Co.
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
Table 1 Examples of common and rare cardiomyopathies
| 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
