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obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay<ref name="Tan-2007">{{Cite journal  | last1 = Tan | first1 = TY. | last2 = Amor | first2 = DJ. | title = Obesity, hypothyroidism, craniosynostosis, cardiac hypertrophy, colitis, and developmental delay: a novel syndrome. | journal = Am J Med Genet A | volume = 143 | issue = 2 | pages = 114-8 | month = Jan | year = 2007 | doi = 10.1002/ajmg.a.31548 | PMID = 17163533 }}</ref>,
obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay<ref name="Tan-2007">{{Cite journal  | last1 = Tan | first1 = TY. | last2 = Amor | first2 = DJ. | title = Obesity, hypothyroidism, craniosynostosis, cardiac hypertrophy, colitis, and developmental delay: a novel syndrome. | journal = Am J Med Genet A | volume = 143 | issue = 2 | pages = 114-8 | month = Jan | year = 2007 | doi = 10.1002/ajmg.a.31548 | PMID = 17163533 }}</ref>,
[[prolonged QT syndrome]],  
[[prolonged QT syndrome]],  
X-linked dilated cardiomyopathy,  
X-linked dilated cardiomyopathy<ref name="Towbin-1993">{{Cite journal  | last1 = Towbin | first1 = JA. | last2 = Hejtmancik | first2 = JF. | last3 = Brink | first3 = P. | last4 = Gelb | first4 = B. | last5 = Zhu | first5 = XM. | last6 = Chamberlain | first6 = JS. | last7 = McCabe | first7 = ER. | last8 = Swift | first8 = M. | title = X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. | journal = Circulation | volume = 87 | issue = 6 | pages = 1854-65 | month = Jun | year = 1993 | doi =  | PMID = 8504498 }}</ref>, X-linked fatal infantile cardiomyopathy<ref name="Gedeon-1995">{{Cite journal  | last1 = Gedeon | first1 = AK. | last2 = Wilson | first2 = MJ. | last3 = Colley | first3 = AC. | last4 = Sillence | first4 = DO. | last5 = Mulley | first5 = JC. | title = X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. | journal = J Med Genet | volume = 32 | issue = 5 | pages = 383-8 | month = May | year = 1995 | doi =  | PMID = 7616547 }}</ref>
X-linked fatal infantile cardiomyopathy
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| '''Dermatologic'''
| '''Dermatologic'''
|bgcolor="Beige"|  
|bgcolor="Beige"|  
Familial cutaneous collagenoma,  
Familial cutaneous collagenoma<ref name="Dawn-">{{Cite journal  | last1 = Dawn | first1 = ME. | last2 = Deng | first2 = AC. | last3 = Petrali | first3 = J. | last4 = Wessely | first4 = C. | last5 = Jaffe | first5 = D. | last6 = Gaspari | first6 = AA. | title = Familial cutaneous collagenoma. | journal = Skinmed | volume = 7 | issue = 1 | pages = 43-5 | month =  | year =  | doi =  | PMID = 18174804 }}</ref>,  
[[lentiginosis]],  
[[lentiginosis]],  
[[dermatomyositis]],  
[[dermatomyositis]],  
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[[Oculofaciocardiodental syndrome|syndromic microphthalmia type 7]],  
[[Oculofaciocardiodental syndrome|syndromic microphthalmia type 7]],  
[[WAGR syndrome]],   
[[WAGR syndrome]],   
X-linked dilated cardiomyopathy,  
X-linked dilated cardiomyopathy<ref name="Towbin-1993">{{Cite journal  | last1 = Towbin | first1 = JA. | last2 = Hejtmancik | first2 = JF. | last3 = Brink | first3 = P. | last4 = Gelb | first4 = B. | last5 = Zhu | first5 = XM. | last6 = Chamberlain | first6 = JS. | last7 = McCabe | first7 = ER. | last8 = Swift | first8 = M. | title = X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. | journal = Circulation | volume = 87 | issue = 6 | pages = 1854-65 | month = Jun | year = 1993 | doi =  | PMID = 8504498 }}</ref>,  
X-linked fatal infantile cardiomyopathy,  
X-linked fatal infantile cardiomyopathy<ref name="Gedeon-1995">{{Cite journal  | last1 = Gedeon | first1 = AK. | last2 = Wilson | first2 = MJ. | last3 = Colley | first3 = AC. | last4 = Sillence | first4 = DO. | last5 = Mulley | first5 = JC. | title = X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. | journal = J Med Genet | volume = 32 | issue = 5 | pages = 383-8 | month = May | year = 1995 | doi =  | PMID = 7616547 }}</ref>, [[Yunis-Varon syndrome]]  
[[Yunis-Varon syndrome]]  
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*[[Fabry disease]]
*[[Fabry disease]]
*[[Familial cardiomyopathy]]
*[[Familial cardiomyopathy]]
*Familial cutaneous collagenoma
*Familial cutaneous collagenoma<ref name="Dawn-">{{Cite journal  | last1 = Dawn | first1 = ME. | last2 = Deng | first2 = AC. | last3 = Petrali | first3 = J. | last4 = Wessely | first4 = C. | last5 = Jaffe | first5 = D. | last6 = Gaspari | first6 = AA. | title = Familial cutaneous collagenoma. | journal = Skinmed | volume = 7 | issue = 1 | pages = 43-5 | month =  | year =  | doi =  | PMID = 18174804 }}</ref>
*[[Cardiomyopathy|Familial hypertrophic cardiomyopathy]]
*[[Cardiomyopathy|Familial hypertrophic cardiomyopathy]]
*[[Fenfluramine]]
*[[Fenfluramine]]
Line 657: Line 655:
*[[Whipple's disease]]
*[[Whipple's disease]]
*[[Wolfram syndrome]]
*[[Wolfram syndrome]]
*X-linked dilated cardiomyopathy
*X-linked dilated cardiomyopathy<ref name="Towbin-1993">{{Cite journal  | last1 = Towbin | first1 = JA. | last2 = Hejtmancik | first2 = JF. | last3 = Brink | first3 = P. | last4 = Gelb | first4 = B. | last5 = Zhu | first5 = XM. | last6 = Chamberlain | first6 = JS. | last7 = McCabe | first7 = ER. | last8 = Swift | first8 = M. | title = X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. | journal = Circulation | volume = 87 | issue = 6 | pages = 1854-65 | month = Jun | year = 1993 | doi =  | PMID = 8504498 }}</ref>
*X-linked fatal infantile cardiomyopathy
*X-linked fatal infantile cardiomyopathy<ref name="Gedeon-1995">{{Cite journal  | last1 = Gedeon | first1 = AK. | last2 = Wilson | first2 = MJ. | last3 = Colley | first3 = AC. | last4 = Sillence | first4 = DO. | last5 = Mulley | first5 = JC. | title = X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. | journal = J Med Genet | volume = 32 | issue = 5 | pages = 383-8 | month = May | year = 1995 | doi =  | PMID = 7616547 }}</ref>
*[[Yunis-Varon syndrome]]
*[[Yunis-Varon syndrome]]
{{col-end}}
{{col-end}}

Revision as of 08:22, 14 August 2013

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ayokunle Olubaniyi, M.B,B.S [2]

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

Life-threatening causes include conditions which result in death or permanent disability within 24 hours if left untreated.

Common Causes

Causes by Organ System

Cardiovascular

Arrhythmogenic right ventricular dysplasia, arterial calcification of infancy, Brugada syndrome, cardiac transplant rejection, cardiomyopathy-renal anomalies[1], chronic tachycardia, coronary artery disease, cytochrome c oxidase deficiency, endomyocardial fibrosis, eosinophilic endomyocardial disease, giant cell myocarditis, hypertension, Keshan disease, left ventricular noncompaction, Loeffler endocarditis, myocarditis, Naxos disease, obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay[2], prolonged QT syndrome, X-linked dilated cardiomyopathy[3], X-linked fatal infantile cardiomyopathy[4]

Chemical / poisoning

Arsenic, cobalt, endothall, ethanol, lead, thallium, allylamine, carbon monoxide, toxic mushrooms

Dermatologic

Familial cutaneous collagenoma[5], lentiginosis, dermatomyositis, Carvajal-Huerta syndrome, Hand-Schuller-Christian syndrome, McLeod syndrome, multiple lentigines syndrome, Naxos disease, pityriasis lichenoides et varioliformis acuta (PLEVA), Refsum disease

Drug Side Effect

5-fluorouracil, aclarubicin, actinomycin D, alemtuzumab, amrubicin, bleomycin, certolizumab pegol, cisplatin, clozapine, cyclophosphamide, dasatinib, daunorubicin, disopyramide, doxorubicin, epirubicin, fenfluramine, hydralazine, idarubicin, imatinib, interferon-alpha, mitoxantrone, paclitaxel, paracetamol, pirarubicin, pixantrone, streptomycin, sunitinib, tacrolimus, trastuzumab, tricyclic anti-depressant abuse, valrubicin

Ear Nose Throat No underlying causes
Endocrine

Acromegaly, amyloidosis, carcinoid syndrome, celiac disease, cushing syndrome, diabetes Mellitus, gout, hemochromatosis, hyperparathyroidism, hyperthyroidism, hypothyroidism, obesity-colitis-hypothyroidism-cardiac hypertrophy developmental delay[2], paraneoplastic syndromes, pheochromocytoma, pituitary tumor, WAGR syndrome, Whipple's disease

Environmental Heatstroke, hypothermia, lightning strike, radiation
Gastroenterologic Hemochromatosis, obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay complex[2], Whipple's Disease
Genetic

Alpers' disease, Brugada syndrome, Carvajal-Huerta syndrome, chromosome 11, partial deletion, congenital disorders of glycosylation, congenital generalized lipodystrophy, Costello syndrome, cytochrome c oxidase deficiency Desmin-related myofibrillar myopathy, Emery-Dreifuss muscular dystrophy, familial cardiomyopathy, Friedreich's ataxia, hereditary spherocytosis, Hurler syndrome, Hutchinson-Gilford progeria syndrome, hypertrichotic osteochondrodysplasia, Keshan disease, Laing distal myopathy, LAMA2-related muscular dystrophy, mitochondrial trifunctional protein deficiency, multiple lentigines syndrome, muscular dystrophy, Naxos disease, Noonan syndrome, porphyria, prolonged QT syndrome, pseudoxanthoma elasticum, Refsum disease, Salih myopathy, sarcoglycanopathy, syndromic microphthalmia type 7, WAGR syndrome, X-linked dilated cardiomyopathy[3], X-linked fatal infantile cardiomyopathy[4], Yunis-Varon syndrome

Hematologic Hereditary spherocytosis
Iatrogenic Cardiac irradiation
Infectious Disease

Adenovirus, African trypanosomiasis, arbovirus, ascariasis, Aspergillosis, Beta-hemolytic streptococci, blastomycosis, brucella, Chagas disease, coccidioidomycosis, coxsackie A virus, coxsackie virus B1-B5, cryptococcosis, cysticercosis, cytomegalovirus, diptheria, echovirus, enterococci, Epstein-Barr virus (EBV), filariasis, flavivirus, histoplasmosis, HIV, influenza, leishmaniasis, leptospirosis, loeffler endocarditis, Lyme disease, malaria, measles, mumps, pertussis, poliomyelitis, psittacosis, Q fever, rabies, rheumatic fever, rocky mountain spotted fever, sarcosporidiosis, schistosomiasis, staphylococcus, syphilis, tetanus, toxoplasmosis, trichinosis, tuberculosis, typhoid fever, varicella-zoster virus

Musculoskeletal / Ortho

Arthrogryposis due to muscular dystrophy, cytochrome c oxidase deficiency, dermatomyositis, duchenne muscular dystrophy, Emery-Dreifuss muscular dystrophy, Hand-Schuller-Christian Syndrome, Kearns-Sayre syndrome, mitochondrial myopathy, muscular dystrophy, myotonic dystrophy

Neurologic

Alpers' disease, d-2-hydroxyglutarate dehydrogenase deficiency, Friedreich's ataxia, Hand-Schuller-Christian Syndrome, Kearns-Sayre syndrome, MELAS syndrome Whipple's disease

Nutritional / Metabolic

3-hydroxyacyl-CoA dehydrogenase deficiency, beriberi , carbohydrate deficient glycoprotein syndrome type 1a, carnitine deficiency, Coenzyme Q10 (CoQ10) deficiency, coenzyme Q cytochrome c reductase deficiency, congenital disorder of glycosylation, cytochrome C Oxidase deficiency, d-2-hydroxyglutarate dehydrogenase deficiency, Fabry disease, gangliosidosis, Gaucher's disease, glutaric acidemia type 2, gout, hemochromatosis, Hunter syndrome, Hurler syndrome, Isobutyryl-coenzyme A dehydrogenase deficiency, Keshan disease, kwashiorkor, long-chain Acyl CoA dehydrogenase deficiency, malonic aciduria, MELAS syndrome, mitochondrial trifunctional protein deficiency, mucopolysaccharidoses, Niemann-Pick disease, niacin deficiency, oxalosis, paraneoplastic syndromes, Pompe disease, porphyria, Refsum disease, respiratory chain complex I deficiency, s-adenosylhomocysteine hydrolase deficiency, scurvy, selenium deficiency, Subacute necrotising encephalomyelopathy, triosephosphate isomerase deficiency, Uremia, vitamin B deficiency, vitamin D overdose

Obstetric/Gynecologic Peripartum cardiomyopathy
Oncologic

Angioma, myxomas, pituitary tumour, rhabdomyoma, sarcoma, leukemia, WAGR syndrome, carcinoid syndrome

Opthalmologic

Hand-Schuller-Christian syndrome, Syndromic microphthalmia type 7, myotonic dystrophy, WAGR syndrome

Overdose / Toxicity

Alcohol, cobalt poisoning, cocaine abuse, oxalosis, paracetamol, tricyclic antidepressant, vitamin D overdose

Psychiatric Takotsubo cardiomyopathy
Pulmonary No underlying causes
Renal / Electrolyte

Cardiomyopathy-renal anomalies[1], hypocalcemia, hypokalemia, hypomagnesemia, uremia, WAGR syndrome, MELAS syndrome

Rheum / Immune / Allergy

Gout, Kawasaki disease, polyarteritis nodosa, rheumatoid arthritis, systemic sclerosis, scleroderma, systemic lupus erythematosus

Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Dental No underlying causes
Miscellaneous

Black widow spider bite, cardiac transplant rejection, idiopathic dilated cardiomyopathy, mitochondrial trifunctional protein deficiency, obesity, obstructive sleep apnea, stress-induced cardiomyopathy

Causes in Alphabetical Order

Cardiomyopathies and Genetics

Genetic causes of cardiomyopathies.[6]

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

References

  1. ↑ 1.0 1.1 1.2 Leask, KM.; Kerr, B.; Ladusans, E. (2007). "Cardiomyopathy with renal anomalies in two siblings: a new recessive syndrome?". Clin Dysmorphol. 16 (1): 51–3. doi:10.1097/MCD.0b013e328010caa9. PMID 17159516. Unknown parameter |month= ignored (help)
  2. ↑ 2.0 2.1 2.2 2.3 Tan, TY.; Amor, DJ. (2007). "Obesity, hypothyroidism, craniosynostosis, cardiac hypertrophy, colitis, and developmental delay: a novel syndrome". Am J Med Genet A. 143 (2): 114–8. doi:10.1002/ajmg.a.31548. PMID 17163533. Unknown parameter |month= ignored (help)
  3. ↑ 3.0 3.1 3.2 Towbin, JA.; Hejtmancik, JF.; Brink, P.; Gelb, B.; Zhu, XM.; Chamberlain, JS.; McCabe, ER.; Swift, M. (1993). "X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus". Circulation. 87 (6): 1854–65. PMID 8504498. Unknown parameter |month= ignored (help)
  4. ↑ 4.0 4.1 4.2 Gedeon, AK.; Wilson, MJ.; Colley, AC.; Sillence, DO.; Mulley, JC. (1995). "X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome". J Med Genet. 32 (5): 383–8. PMID 7616547. Unknown parameter |month= ignored (help)
  5. ↑ 5.0 5.1 Dawn, ME.; Deng, AC.; Petrali, J.; Wessely, C.; Jaffe, D.; Gaspari, AA. "Familial cutaneous collagenoma". Skinmed. 7 (1): 43–5. PMID 18174804.
  6. ↑ Towbin JA, Bowles NE (2002). "The failing heart". Nature. 415 (6868): 227–33. doi:10.1038/415227a. PMID 11805847. Unknown parameter |month= ignored (help)

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