Cardiomyopathy causes: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Cardiomyopathy}} | {{Cardiomyopathy}} | ||
{{CMG}} | {{CMG}} | ||
==Overview== | ==Overview== | ||
There is a very wide range of factors that can cause cardiomyopathy, ranging from infectious causes, | There is a very wide range of factors that can cause cardiomyopathy, ranging from [[infectious]] causes, [[toxin]]s, [[genetic]] causes and other disease processes. | ||
==Causes== | ==Causes== | ||
=== | ===Common Causes=== | ||
* [[Alcoholism]] | * [[Alcoholism]] | ||
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===Causes by Organ System=== | ===Causes by Organ System=== | ||
{|style="width:80%; height:100px" border="1" | {|style="width:80%; height:100px" border="1" | ||
|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular''' | |style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular''' | ||
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
{{ | {{MultiCol}} | ||
* [[3-methylglutaconic aciduria]], type 4 | * [[3-methylglutaconic aciduria]], type 4 | ||
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* [[Hypocalcemia]] | * [[Hypocalcemia]] | ||
{{ | {{ColBreak}} | ||
* [[Hypokalemia]] | * [[Hypokalemia]] | ||
* [[Hypomagnesemia]] | * [[Hypomagnesemia]] | ||
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* [[Malaria]] | * [[Malaria]] | ||
* [[Malonic aciduria]] | * [[Malonic aciduria]] | ||
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* X-linked - fatal infantile Cardiomyopathy | * X-linked - fatal infantile Cardiomyopathy | ||
{{ | {{EndMultiCol}} | ||
=== Genetic Causes of Cardiomyopathy=== | === Genetic Causes of Cardiomyopathy=== | ||
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==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
{{WH}} | |||
{{WS}} | |||
[[Category: | [[Category:Best pages]] | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
[[Category:Genetic Disease]] | [[Category:Genetic Disease]] | ||
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[[Category:Up-To-Date cardiology]] | [[Category:Up-To-Date cardiology]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 00:50, 9 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]
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
Common Causes
- Beri-Beri (thiamine or vitamin B1)
- Cocaine abuse
Causes by Organ System
Causes in 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