Congenital heart disease causes: Difference between revisions
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*[[Aortic stenosis]] | *[[Aortic stenosis]] | ||
*[[Assisted reproductive technology]] | *[[Assisted reproductive technology]] | ||
*[[Atrial septal defect]] | *[[Atrial septal defect]] <ref name="pmid24012023">{{cite journal| author=Zheng JY, Tian HT, Zhu ZM, Li B, Han L, Jiang SL et al.| title=Prevalence of symptomatic congenital heart disease in Tibetan school children. | journal=Am J Cardiol | year= 2013 | volume= 112 | issue= 9 | pages= 1468-70 | pmid=24012023 | doi=10.1016/j.amjcard.2013.07.028 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24012023 }} </ref> | ||
*[[Atrioventricular septal defect]] <ref name="pmid24702954">{{cite journal| author=Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S et al.| title=Rare variants in NR2F2 cause congenital heart defects in humans. | journal=Am J Hum Genet | year= 2014 | volume= 94 | issue= 4 | pages= 574-85 | pmid=24702954 | doi=10.1016/j.ajhg.2014.03.007 | pmc=PMC3980509 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24702954 }} </ref> | *[[Atrioventricular septal defect]] <ref name="pmid24702954">{{cite journal| author=Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S et al.| title=Rare variants in NR2F2 cause congenital heart defects in humans. | journal=Am J Hum Genet | year= 2014 | volume= 94 | issue= 4 | pages= 574-85 | pmid=24702954 | doi=10.1016/j.ajhg.2014.03.007 | pmc=PMC3980509 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24702954 }} </ref> | ||
*Barrow-Fitzsimmons syndrome | *Barrow-Fitzsimmons syndrome | ||
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*Hurst-Hallam-Hockey syndrome | *Hurst-Hallam-Hockey syndrome | ||
*[[Hydantoin]] | *[[Hydantoin]] | ||
*[[Hypoplastic left heart syndrome]] | *[[Hypoplastic left heart syndrome]] <ref name="pmid23979609">{{cite journal| author=Warburton D, Ronemus M, Kline J, Jobanputra V, Williams I, Anyane-Yeboa K et al.| title=The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease. | journal=Hum Genet | year= 2014 | volume= 133 | issue= 1 | pages= 11-27 | pmid=23979609 | doi=10.1007/s00439-013-1353-9 | pmc=PMC3880624 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23979609 }} </ref> | ||
*[[Ibuprofen]] | *[[Ibuprofen]] | ||
*[[Isotretinoin]] | *[[Isotretinoin]] | ||
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*[[Noonan syndrome]] | *[[Noonan syndrome]] | ||
*[[Organic solvents]] | *[[Organic solvents]] | ||
*[[Patent ductus arteriosus]] | *[[Patent ductus arteriosus]] <ref name="pmid24012023">{{cite journal| author=Zheng JY, Tian HT, Zhu ZM, Li B, Han L, Jiang SL et al.| title=Prevalence of symptomatic congenital heart disease in Tibetan school children. | journal=Am J Cardiol | year= 2013 | volume= 112 | issue= 9 | pages= 1468-70 | pmid=24012023 | doi=10.1016/j.amjcard.2013.07.028 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24012023 }} </ref> | ||
{{col-break|width=33%}} | {{col-break|width=33%}} | ||
*[[Pfeiffer syndrome|Pfeiffer syndrome type III]] | *[[Pfeiffer syndrome|Pfeiffer syndrome type III]] | ||
| Line 211: | Line 211: | ||
*[[Sakati syndrome]] | *[[Sakati syndrome]] | ||
*[[Systemic lupus erythematosus]] <ref name="pmid24342193">{{cite journal| author=Quan MY, Wang DH| title=[Clinical features of preterm infants born to mothers with systemic lupus erythematosus: a retrospective analysis]. | journal=Zhongguo Dang Dai Er Ke Za Zhi | year= 2013 | volume= 15 | issue= 12 | pages= 1045-9 | pmid=24342193 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24342193 }} </ref> | *[[Systemic lupus erythematosus]] <ref name="pmid24342193">{{cite journal| author=Quan MY, Wang DH| title=[Clinical features of preterm infants born to mothers with systemic lupus erythematosus: a retrospective analysis]. | journal=Zhongguo Dang Dai Er Ke Za Zhi | year= 2013 | volume= 15 | issue= 12 | pages= 1045-9 | pmid=24342193 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24342193 }} </ref> | ||
*[[Tetralogy of Fallot]] | *[[Tetralogy of Fallot]] <ref name="pmid24000169">{{cite journal| author=Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM et al.| title=GATA4 loss-of-function mutations underlie familial tetralogy of fallot. | journal=Hum Mutat | year= 2013 | volume= 34 | issue= 12 | pages= 1662-71 | pmid=24000169 | doi=10.1002/humu.22434 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24000169 }} </ref> | ||
*[[Thalidomide]] | *[[Thalidomide]] | ||
*[[Total anomalous pulmonary venous connection]] | *[[Total anomalous pulmonary venous connection]] | ||
Revision as of 16:57, 5 November 2014
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Congenital heart disease Microchapters |
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Differentiating Congenital heart disease from other Disorders |
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Congenital heart disease causes On the Web |
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American Roentgen Ray Society Images of Congenital heart disease causes |
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Risk calculators and risk factors for Congenital heart disease causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Priyamvada Singh, MBBS [2] Ogheneochuko Ajari, MB.BS, MS [3] Assistant Editor-In-Chief: Kristin Feeney, B.S. [4]
Overview
Current knowledge regarding the causes of congenital heart disease is limited. Most research has been based on small studies (<1,000 patients). As is common with many congenital related conditions, there are gaps in knowledge regarding the causation of congenital heart disease. Congenital heart disease is multi-factorial in origin, with genetics and environmental factors both playing a role.
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
- Aortic stenosis
- Atrial septal defect[1]
- Coarctation of the aorta
- Down syndrome[2]
- Ebstein's anomaly
- Endocardial cushion defect
- Hypoplastic left heart syndrome
- Noonan syndrome[2]
- Patent ductus arteriosus
- Pulmonary atresia
- Pulmonic stenosis
- Tetralogy of Fallot
- Total anomalous pulmonary venous connection
- Transposition of the great vessels
- Turner syndrome
- Ventricular septal defect
Causes by Organ System
| Cardiovascular | No underlying causes |
| Chemical / poisoning | No underlying causes |
| Dermatologic | No underlying causes |
| Drug Side Effect | No underlying causes |
| Ear Nose Throat | No underlying causes |
| Endocrine | No underlying causes |
| Environmental | No underlying causes |
| Gastroenterologic | No underlying causes |
| Genetic | No underlying causes |
| Hematologic | No underlying causes |
| Iatrogenic | No underlying causes |
| Infectious Disease | No underlying causes |
| Musculoskeletal / Ortho | No underlying causes |
| Neurologic | No underlying causes |
| Nutritional / Metabolic | No underlying causes |
| Obstetric/Gynecologic | No underlying causes |
| Oncologic | No underlying causes |
| Opthalmologic | No underlying causes |
| Overdose / Toxicity | No underlying causes |
| Psychiatric | No underlying causes |
| Pulmonary | No underlying causes |
| Renal / Electrolyte | No underlying causes |
| Rheum / Immune / Allergy | No underlying causes |
| Sexual | No underlying causes |
| Trauma | No underlying causes |
| Urologic | No underlying causes |
| Dental | No underlying causes |
| Miscellaneous | No underlying causes |
Causes in Alphabetical Order
References
- ↑ Liu JJ, Fan LL, Chen JL, Tan ZP, Yang YF (2014). "A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect". J Zhejiang Univ Sci B. 15 (9): 830–7. doi:10.1631/jzus.B1400062. PMC 4162884. PMID 25183037.
- ↑ 2.0 2.1 Prendiville TW, Gauvreau K, Tworog-Dube E, Patkin L, Kucherlapati RS, Roberts AE; et al. (2014). "Cardiovascular disease in Noonan syndrome". Arch Dis Child. 99 (7): 629–34. doi:10.1136/archdischild-2013-305047. PMID 24534818.
- ↑ 3.0 3.1 Zheng JY, Tian HT, Zhu ZM, Li B, Han L, Jiang SL; et al. (2013). "Prevalence of symptomatic congenital heart disease in Tibetan school children". Am J Cardiol. 112 (9): 1468–70. doi:10.1016/j.amjcard.2013.07.028. PMID 24012023.
- ↑ Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S; et al. (2014). "Rare variants in NR2F2 cause congenital heart defects in humans". Am J Hum Genet. 94 (4): 574–85. doi:10.1016/j.ajhg.2014.03.007. PMC 3980509. PMID 24702954.
- ↑ Opotowsky AR, Landzberg MJ, Beghetti M (2014). "The exceptional and far-flung manifestations of heart failure in Eisenmenger syndrome". Heart Fail Clin. 10 (1): 91–104. doi:10.1016/j.hfc.2013.09.005. PMID 24275297.
- ↑ Warburton D, Ronemus M, Kline J, Jobanputra V, Williams I, Anyane-Yeboa K; et al. (2014). "The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease". Hum Genet. 133 (1): 11–27. doi:10.1007/s00439-013-1353-9. PMC 3880624. PMID 23979609.
- ↑ Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF; et al. (2002). "Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24". J Med Genet. 39 (7): 478–83. PMC 1735188. PMID 12114478.
- ↑ Quan MY, Wang DH (2013). "[Clinical features of preterm infants born to mothers with systemic lupus erythematosus: a retrospective analysis]". Zhongguo Dang Dai Er Ke Za Zhi. 15 (12): 1045–9. PMID 24342193.
- ↑ Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM; et al. (2013). "GATA4 loss-of-function mutations underlie familial tetralogy of fallot". Hum Mutat. 34 (12): 1662–71. doi:10.1002/humu.22434. PMID 24000169.
- ↑ Cunningham BK, Hadley DW, Hannoush H, Meltzer AC, Niforatos N, Pineda-Alvarez D; et al. (2013). "Analysis of cardiac anomalies in VACTERL association". Birth Defects Res A Clin Mol Teratol. 97 (12): 792–7. doi:10.1002/bdra.23211. PMID 24343877.
- ↑ Al-Farqani A, Panduranga P, Al-Maskari S, Thomas E (2013). "VACTERL association with double-chambered left ventricle: A rare occurrence". Ann Pediatr Cardiol. 6 (2): 200–1. doi:10.4103/0974-2069.115283. PMC 3957460. PMID 24688248.