Dextrocardia pathophysiology
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
The exact pathogenesis of dextrocardia is not fully understood. The malposition is not as a result of any extracardiac abnormalities but intrinsic to the heart. It is as a result of embryological abnormalities that occur during the development of the heart. Genes involved in the pathogenesis of dextrocardia include: ZIC3, ACVR2B, NODAL.
Pathophysiology
Embryology
Pathogenesis
Genetics
Associated Conditions
Conditions associated with [disease name] include:[1][2][3][4]
- Tricuspid atresia
- Transposition of the great vessels
- Pulmonary stenosis
- Double-outlet double-inlet ventricle
- Single ventricle
- Sick sinus syndrome
- Situs inversus
- Situs solitus
- Situs ambiguous
- Kartagener syndrome
- Double-outlet or double-inlet ventricles
References
- ↑ Khoury M, Harbieh B, Heriopian A (2013). "Isolated dextrocardia and congenital heart blocking". Radiol Case Rep. 8 (1): 521. doi:10.2484/rcr.v8i1.521. PMC 4900208. PMID 27330607.
- ↑ Panneerselvam A, Subbiahnadar P (2012). "Is it dextrocardia or dextroversion?". BMJ Case Rep. 2012. doi:10.1136/bcr.01.2012.5493. PMC 3316784. PMID 22605582.
- ↑ Ogunlade O, Ayoka AO, Akomolafe RO, Akinsomisoye OS, Irinoye AI, Ajao A; et al. (2015). "The role of electrocardiogram in the diagnosis of dextrocardia with mirror image atrial arrangement and ventricular position in a young adult Nigerian in Ile-Ife: a case report". J Med Case Rep. 9: 222. doi:10.1186/s13256-015-0695-4. PMC 4584464. PMID 26411880.
- ↑ Maldjian, Pierre D.; Saric, Muhamed (2007). "Approach to Dextrocardia in Adults:Review". American Journal of Roentgenology. 188 (6_supplement): S39–S49. doi:10.2214/AJR.06.1179. ISSN 0361-803X.