Cardiomyopathy causes: Difference between revisions
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| '''Musculoskeletal / Ortho''' | | '''Musculoskeletal / Ortho''' | ||
|bgcolor="Beige"| [[Dermatomyositis]], [[Arthrogryposis due to muscular dystrophy]], [[Duchenne muscular dystrophy]], [[Emery-Dreifuss muscular dystrophy]], [[Limb girdle muscular dystrophy]], [[Mitochondrial myopathy]], [[Muscular Dystrophy]], [[Myotonic dystrophy]], | |bgcolor="Beige"| [[Dermatomyositis]], [[Arthrogryposis due to muscular dystrophy]], [[Duchenne muscular dystrophy]], [[Emery-Dreifuss muscular dystrophy]], [[Limb girdle muscular dystrophy]], [[Mitochondrial myopathy]], [[Muscular Dystrophy]], [[Myotonic dystrophy]], Recessive type Metaphyseal chondrodysplasia, [[Kearns-Sayre Syndrome]], Cardiomyopathy with myopathy due to COX deficency, Facio-cardio-musculo-skeletal syndrome, [[Hand-Schuller-Christian Syndrome]] | ||
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| '''Opthalmologic''' | | '''Opthalmologic''' | ||
|bgcolor="Beige"| [[Hand-Schuller-Christian Syndrome]], | |bgcolor="Beige"| [[Hand-Schuller-Christian Syndrome]], Microphthalmia, syndromic 7, [[Myotonic dystrophy]], [[WAGR Syndrome]] | ||
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| '''Miscellaneous''' | | '''Miscellaneous''' | ||
|bgcolor="Beige"| [[Cocaine]] abuse, [[Alcoholism]], [[Amyloidosis]], [[Electric shock]], [[Idiopathic dilated cardiomyopathy]], [[Immunoglobulinic amyloidosis]], [[Irradiation]], [[Mitochondrial trifunctional protein deficiency]], [[Obesity]], [[physically and physiologically stress induced (tako-tsubo syndrome or "broken heart syndrome")]], | |bgcolor="Beige"| [[Cocaine]] abuse, [[Alcoholism]], [[Amyloidosis]], [[Electric shock]], [[Idiopathic dilated cardiomyopathy]], [[Immunoglobulinic amyloidosis]], [[Irradiation]], [[Mitochondrial trifunctional protein deficiency]], [[Obesity]], [[physically and physiologically stress induced (tako-tsubo syndrome or "broken heart syndrome")]], Toxic mushrooms -- cyclopeptides | ||
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Revision as of 19:10, 3 January 2013
Cardiomyopathy Microchapters |
Diagnosis |
---|
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]
Causes
Common Causes
- Beri-Beri (thiamine or vitamin B1)
- Cocaine abuse
Causes by Organ System
Causes in Alphabetical Order
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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