Cardiomyopathy causes: Difference between revisions
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==Most common== | ==Most common== | ||
==By organ system== | ==By organ system== | ||
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|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular''' | |style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular''' | ||
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | [[Arrhythmogenic right ventricular dysplasia]], [[Arterial calcification of infancy]], [[Brugada syndrome]], [[Cardiac transplant rejection]], [[Cardiomyopathy - diabetes - deafness]], [[Cardiomyopathy -- hypogonadism -- metabolic anomalies complex]], [[Cardiomyopathy -- renal anomalies]], [[Cardiomyopathy -- spherocytosis]], [[Cardiomyopathy with myopathy due to COX deficency]], [[Chronic tachycardia]], [[Congenital heart defect]], [[Coronary artery disease]], [[Endomyocardial fibrosis]], [[Eosinophilic endomyocardial disease]], [[Facio-cardio-musculo-skeletal syndrome]], [[Giant Cell Myocarditis | |style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | [[Arrhythmogenic right ventricular dysplasia]], [[Arterial calcification of infancy]], [[Brugada syndrome]], [[Cardiac transplant rejection]], [[Cardiomyopathy - diabetes - deafness]], [[Cardiomyopathy -- hypogonadism -- metabolic anomalies complex]], [[Cardiomyopathy -- renal anomalies]], [[Cardiomyopathy -- spherocytosis]], [[Cardiomyopathy with myopathy due to COX deficency]], [[Chronic tachycardia]], [[Congenital heart defect]], [[Coronary artery disease]], [[Endomyocardial fibrosis]], [[Eosinophilic endomyocardial disease]], [[Facio-cardio-musculo-skeletal syndrome]], [[Giant Cell Myocarditis]], [[Inflammatory myocarditis]], [[Kawasaki's Disease]], [[Myocarditis]], [[Poorly controlled hypertension]], [[Prolonged QT syndrome]], [[Rheumatic Fever]], [[Loeffler endocarditis]], [[Keshan disease]], [[Obesity -- colitis -- hypothyroidism -- cardiac hypertrophy -- developmental delay]], [[Myotonic dystrophy]] | ||
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* [[Electric shock]] | * [[Electric shock]] | ||
* [[Electrolyte | * [[Electrolyte imbalance]] | ||
* [[Emery-Dreifuss muscular dystrophy]] | * [[Emery-Dreifuss muscular dystrophy]] | ||
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* [[Limb girdle muscular dystrophy]] | * [[Limb girdle muscular dystrophy]] | ||
* [[Loeffler endocarditis]] | * [[Loeffler endocarditis]] | ||
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* [[Refsum's disease]] | * [[Refsum's disease]] | ||
* [[ | * [[Rhabdomyoma]] | ||
* [[Rheumatic Fever]] | * [[Rheumatic Fever]] | ||
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* [[Rocky Mountain Spotted Fever]] | * [[Rocky Mountain Spotted Fever]] | ||
* [[ | * [[Sarcosporidiosis]] | ||
* [[Sarcoglycanopathy]] | * [[Sarcoglycanopathy]] | ||
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* [[Trichinosis]] | * [[Trichinosis]] | ||
* [[Tricyclic anti-depressant | * [[Tricyclic anti-depressant]] abuse | ||
* [[Triosephosphate isomerase deficiency]] | * [[Triosephosphate isomerase deficiency]] | ||
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* [[Vitamin B deficiency]] | * [[Vitamin B deficiency]] | ||
* [[Vitamin D | * [[Vitamin D]] overdose | ||
* [[WAGR Syndrome]] | * [[WAGR Syndrome]] |
Revision as of 17:15, 10 July 2012
Cardiomyopathy Microchapters |
Diagnosis |
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Treatment |
Guidelines |
2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy |
Case Studies |
Cardiomyopathy causes On the Web |
American Roentgen Ray Society Images of Cardiomyopathy causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Complete Differential Diagnosis of the Causes of Cardiomyopathy
Most common
By organ system
By alphabetical order
|
|
Genetic causes of cardiomyopathy
Phenotype | Inheritance pattern | Chromosomal locus | Gene | Protein | Skeletal myopathy |
---|---|---|---|---|---|
Dilated cardiomyopathy | X-linked | Xp21 | dystrophin | Dystrophin | Duchenne / Becker muscular dystrophy |
X-linked | Xq28 | G4.5 | Tafazzin | Barth syndrome | |
Autosomal dominant | 15q14 | actin | Actin | Nemaline myopathy | |
2q35 | desmin | Desmin | Desmin myopathy | ||
5q33 | δ-sarcoglycan | δ-sarcoglycan | Limb girdle muscular dystrophy 2F | ||
1q32 | Troponin T | Troponin T | |||
14q11 | β-myosin heavy chain | β-myosin heavy chain | |||
15q2 | α-tropomyosin | α-tropomyosin | Nemaline myopathy | ||
Midna | Mitochondrial respiratory chain | Mitochondrial respiratory chain | Mitochondrial myopathy | ||
Dilated cardiomyopathy with conduction disease | Autosomal dominant | 1q21 | lamin A/C | Lamin A/C | Emery-Dreifuss muscular dystrophy |
Hypertrophic cardiomyopathy | Autosomal dominant | 14q11 | β-myosin heavy chain | β-myosin heavy chain | |
14q11 | β-myosin heavy chain | β-myosin heavy chain | |||
1q32 | Troponin T | Troponin T | |||
12q23 | Troponin T | Troponin T | |||
15q2 | α-tropomyosin | α-tropomyosin | Nemaline myopathy | ||
11q11 | myosin-binding protein C | myosin-binding protein C | |||
3p21 | myosin essential light chain | myosin essential light chain | |||
3p21 | myosin regulatory light chain | myosin regulatory light chain | |||
2p31 | titin | Titin | |||
Hypertrophic cardiomyopathy with Wolf-Parkinson-White syndrome | 7q3 | AMPK | AMPK | ||
MIDINA | Mitochondrial respiratory chain | Mitochondrial respiratory chain | Mitochondrial myopathy | ||
Left ventricular noncompaction | X-linked | Xq28 | G4.5 | Tafazzin | Barth syndrome |
Autosomal dominant | 18q12 | α-dystrobrevin | α-dystrobrevin | Muscular dystrophy |
Table from article *"The Failing Heart". Nature. June 15, 2007