Congenital heart disease causes: Difference between revisions
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*[[Assisted reproductive technology]] | *[[Assisted reproductive technology]] | ||
*[[Atrial septal defect]] | *[[Atrial septal defect]] | ||
*[[Atrioventricular septal defect]] | *[[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 | ||
*[[Benzodiazepines]] | *[[Benzodiazepines]] | ||
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*[[Rubella]] | *[[Rubella]] | ||
*[[Sakati syndrome]] | *[[Sakati syndrome]] | ||
*[[Systemic lupus erythematosus]] | *[[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]] | ||
*[[Thalidomide]] | *[[Thalidomide]] | ||
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*[[Truncus arteriosus]] | *[[Truncus arteriosus]] | ||
*[[Turner syndrome]] | *[[Turner syndrome]] | ||
*[[VACTERL association]] | *[[VACTERL association]] <ref name="pmid24343877">{{cite journal| author=Cunningham BK, Hadley DW, Hannoush H, Meltzer AC, Niforatos N, Pineda-Alvarez D et al.| title=Analysis of cardiac anomalies in VACTERL association. | journal=Birth Defects Res A Clin Mol Teratol | year= 2013 | volume= 97 | issue= 12 | pages= 792-7 | pmid=24343877 | doi=10.1002/bdra.23211 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24343877 }} </ref><ref name="pmid24688248">{{cite journal| author=Al-Farqani A, Panduranga P, Al-Maskari S, Thomas E| title=VACTERL association with double-chambered left ventricle: A rare occurrence. | journal=Ann Pediatr Cardiol | year= 2013 | volume= 6 | issue= 2 | pages= 200-1 | pmid=24688248 | doi=10.4103/0974-2069.115283 | pmc=PMC3957460 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24688248 }} </ref> | ||
*[[Ventricular septal defect]] | *[[Ventricular septal defect]] | ||
*[[Williams syndrome]] | *[[Williams syndrome]] | ||
Revision as of 16:45, 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.