Cardiomyopathy causes: Difference between revisions
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==Causes== | ==Causes== | ||
===Life Threatening Causes=== | |||
*List the life-threatening causes here.<font color="white">Causes of {{PAGENAME}} developed by WikiDoc.org, Copyleft 2013. Redistribution without attribution prohibited by law.</font> | |||
===Common Causes=== | ===Common Causes=== | ||
* [[Alcoholism]] | * [[Alcoholism]] | ||
Revision as of 15:02, 8 August 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] Associate Editor(s)-in-Chief: Ayokunle Olubaniyi, M.B,B.S
Overview
There is a very wide range of factors that can cause cardiomyopathy, ranging from infectious causes, toxins, genetic causes and other disease processes.
Causes
Life Threatening Causes
- List the life-threatening causes here.Causes of Cardiomyopathy causes developed by WikiDoc.org, Copyleft 2013. Redistribution without attribution prohibited by law.
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