Cardiomyopathy causes: Difference between revisions
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| '''Neurologic''' | | '''Neurologic''' | ||
|bgcolor="Beige"| [[Friedrich's Ataxia]], [[Kearns-Sayre Syndrome]], [[Whipple's Disease]] | |bgcolor="Beige"| [[Friedrich's Ataxia]], [[Kearns-Sayre Syndrome]], [[Whipple's Disease]] | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" | ||
| '''Nutritional / Metabolic''' | | '''Nutritional / Metabolic''' | ||
|bgcolor="Beige"| | |bgcolor="Beige"| [[3-methylglutaconic aciduria]] type 4, [[Beri-Beri]] (thiamine or vitamin B1), [[Carbohydrate deficient glycoprotein syndrome type 1a]], [[Carnitine deficiency]], [[Carnitine palmitoyltransferase 2 deficiency]], [[Carnitine transporter deficiency]], [[Coenzyme Q 10 (CoQ10) deficiency]], [[Coenzyme Q cytochrome c reductase deficiency]], [[Congenital disorder of glycosylation]], [[Cytochrome C Oxidase deficiency]], [[Fabry's Disease]], [[Gangliosidosis]], [[Gaucher's Disease]], [[Glutaric acidemia]] type 2, [[Glycogen storage diseases]], [[Gout]], [[Hunter's Syndrome]], [[Hurler's Syndrome]], [[Keshan disease]], [[Kwashiorkor]], [[Malonic aciduria]], [[MELAS]], [[Neimann-Pick Disease]], [[Niacin deficiency]], [[Oxalosis]], [[Porphyria]], [[Refsum's disease]], [[scurvy]], [[Triosephosphate isomerase deficiency]], [[Vitamin B deficiency]], [[Vitamin D]] overdose | ||
|- | |- | ||
|-bgcolor="LightSteelBlue" | |-bgcolor="LightSteelBlue" |
Revision as of 15:20, 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