Cardiomyopathy causes: Difference between revisions
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| '''Endocrine''' | | '''Endocrine''' | ||
|bgcolor="Beige"| [[Acromegaly]], [[ | |||
|bgcolor="Beige"| | |||
[[Acromegaly]], | |||
[[amyloidosis]], | |||
[[carcinoid syndrome]], | |||
cardiomyopathy-diabetes-deafness complex, | |||
cardiomyopathy-hypogonadism-metabolic anomalies complex, | |||
[[celiac disease]], | |||
[[cushing syndrome]], | |||
[[diabetes Mellitus]], | |||
[[gout]], | |||
[[hemochromatosis]], | |||
[[hyperparathyroidism]], | |||
[[hyperthyroidism]], | |||
[[hypothyroidism]], | |||
obesity-colitis-hypothyroidism-cardiac hypertrophy developmental delay, | |||
[[paraneoplastic syndromes]], | |||
[[pheochromocytoma]], | |||
[[pituitary tumor]] (growth hormone secreting), | |||
[[WAGR syndrome]], | |||
[[Whipple's disease]], | |||
|- | |- | ||
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| '''Environmental''' | | '''Environmental''' | ||
|bgcolor="Beige"| [[Heatstroke]], [[ | |bgcolor="Beige"| [[Heatstroke]], [[hypothermia]], lightening strike | ||
|- | |- | ||
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Revision as of 17:31, 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